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Conferences on Law & Regulations (past events)

Conferences on Law & Regulations address various topics in the field of law & regulations....

Some of the topics covered in Conferences on Law & Regulations are law, regulation, regulatory, human rights, civil rights, human genetics and law reform.

Conferences on Law & Regulations is intended for attendees interested in law & regulations.

Showing 2134 conferences
WINDMission BSR - Eight nations conference
Jan 2024
Clinical Trial Regulation MasterClass
Dec 2023
Promotional Review Committee Compliance & Best Practices Summit
Dec 2023
KUALA LUMPUR International Conference on Economics, Management, Education, and Law (KEMEL)
Dec 2023
IBA Asset Recovery Conference
Dec 2023
Nordic IPR
Nov 2023
Resourcing Tomorrow
Nov 2023
SAHARA+ Conference
Nov 2023
Implementation of a Successful Technology Transfer Process
Nov 2023
TSAM Amsterdam - The Summit for Asset Management
Nov 2023
international Human Capital Conference
Nov 2023
GreenTree Immigrations FREE Webinar on Canada Immigration and Permanent Residency (PR)
Nov 2023
Passport to Proficiency on the ITAR
Nov 2023
Advanced Forum on Import Compliance & Enforcement
Nov 2023
International Conference on Peace and Conflict Management
Nov 2023
Future C4ISR Summit
Nov 2023
American Association of Clinical Urologists Meeting (AACU)
Oct 2023
ACFE Fraud Conference Canada
Oct 2023
International Conference on Womens Right
Oct 2023
The Financial Innovation Forum
Oct 2023
ACIs Conference on U.S.- China Trade Controls
Oct 2023
RaicesCon
Oct 2023
LegalTech Summit (WLF)
Oct 2023
Export Administration Regulations
Oct 2023
ICD-10 Coding Updates! Effective
Sep 2023
Illinois Renewable Energy Conference
Sep 2023
The Crossroads of International Finance and Public Equity Deals: New trends and financing bottlenecks
Sep 2023
International Conference in Finance, Banking and Accounting (ICFBA)
Sep 2023
International Conference on `Law, Education, Marketing and Management` (BLEMM)
Sep 2023
World Conference on Gender Equality
Jul 2023
The IPR Gorilla Conference Dubai
Jul 2023
HIPAA Business Associate Compliance and Dangers
Jul 2023
Integer Emissions Summit and AdBlue Forum Europe
Jun 2023
CFR Part 11 Guidance for Electronic Records and Electronic Signatures in FDA-Regulated Industries
Jun 2023
FDA`s Medical Device Software Regulation Strategy
Jun 2023
IAIL - Imaging the AI Landscape after the AI Act
Jun 2023
FDI & Foreign Subsidies Regulations
Jun 2023
Solar & Energy Storage Summit
Jun 2023
Transform Payments USA
Jun 2023
IAFNS Summer Science Symposium
Jun 2023
World Legal IP Summit
Jun 2023
Nasal Drug Delivery
May 2023
Pharmaceutical and Medical Device Ethics and Compliance Congress
May 2023
Integer Emissions Summit & AdBlue Forum China
May 2023
PATTAYA International Conference on `Economics, Management, Education, and Law` (EMEL)
May 2023
Heroes of Data Privacy
May 2023
International Conference on Human Rights and Literature
May 2023
The NextGen Payments & RegTech Forum (NPF)
May 2023
IBA Transnational Crime Conference
May 2023
Understanding and Managing Competition Law Compliance
Apr 2023
eCTD Submissions
Apr 2023
Legal Leaders USA
Apr 2023
World Data Transfers and Compliance Summit
Mar 2023
Practitioners` Think Tank on ITC Litigation & Enforcement
Mar 2023
Orphan Drugs 101: The Mini Course
Mar 2023
International Conference on Business and Policy Studies (CONF-BPS)
Feb 2023
The Veterinary Drug Approval Process and FDA Regulatory Oversight
Feb 2023
Clinical Data Disclosure and Transparency Summit
Feb 2023
Public-Private Partnerships
Feb 2023
GCR Live: Law Leaders Global
Feb 2023
ICMLLM : International Conference on Medical Law and Legal Medicine
Jan 2023
Lift Vancouver - Cannabis Conference and Trade Show
Jan 2023
Argus Vehicle Emissions and DEF Summit USA
Dec 2022
World Legal Design & Innovation Summit
Dec 2022
Project Management for Pharma Professionals
Dec 2022
Anti-Financial Crime Summit
Dec 2022
Summit On Investment Opportunities In Kenya, Rwanda And DR Congo
Nov 2022
Risk Data Aggregation and Risk Reporting
Nov 2022
Flagship Conference on Regulatory Compliance for Financial Institutions
Nov 2022
London Forum on Global Economic Sanctions
Nov 2022
Africa Trade & Customs Week Summit
Nov 2022
IP Law Europe Summit
Oct 2022
The International Conference on Family and Spiritual Education (ICFSE)
Oct 2022
Conference on Indigenous Consultation & Engagement Atlantic
Oct 2022
International Conference on Religion and Sustainable Development (ICoReSD)
Oct 2022
Implementation of ISO 13485 MasterClass
Oct 2022
ACFE Asia-Pacific Fraud Conference
Sep 2022
Chemical Industry Regulations
Sep 2022
Product Substance Management & Regulatory Compliance
Sep 2022
International Conference on Business Ethics & Corporate Compliance
Sep 2022
Global Takaful & Re-Takaful Forum
Aug 2022
Change Control Best Practices - Avoiding Unintended Consequences of Changes
Jul 2022
International Conference on Mathematics, Statistics, Education & Law (ICMSEL)
Jul 2022
International Conference on Globalization, Business Management, Ethics and Law (GBMEL)
Jun 2022
Gene Regulation: From Emerging Technologies to New Models
Jun 2022
International Conference on Education, Law, Business & Politics (ICELBP)
Jun 2022
The Future of Data Protection: Effective enforcement in the digital world (EDPS)
Jun 2022
Divorce - A Road Map To New Beginnings
Jun 2022
ISPOR Summit
May 2022
Pharmaceutical Aseptic Processing Forum
May 2022
Managing and Leading an Effective In-House Legal Department
Mar 2022
Injectable Drug Delivery
Mar 2022
African Women Rights and their Role in Sustainable Development (AWRSD)
Mar 2022
Successfully Investigating Deviations
Mar 2022
Building Healthcare Innovation & Design
Feb 2022
Patentability and State of the Art Searching
Feb 2022
DUBAI International Conference on Business, Management, Education & Law (BMEL)
Feb 2022
Advanced CMC MasterClass
Feb 2022
Biological Evaluation of Medical Devices
Feb 2022
The EAAR Conference on New Medical Device Regulations (RMD2022)
Feb 2022
International Technology Law Association (ITechLaw) India Conference
Jan 2022
Supplier and Contract Manufacturer Management
Jan 2022
Mastering Renewable & Alternative Energies
Dec 2021
FDA/CMS Summit
Dec 2021
FDA Pharmaceutical Labeling Boot Camp
Dec 2021
Biostimulants Europe
Dec 2021
Plastics Regulations USA
Dec 2021
Inhaled Drug Delivery
Nov 2021
Effective Contract Management
Nov 2021
Aesthetic & Cosmetic Regulatory Events Summit (ACRAS)
Nov 2021
Forex Expo
Nov 2021
US Safety Data Exchange Agreements (SDEAs) and PV Arrangements with External Vendors MasterClass
Nov 2021
The Art of European Claim Drafting
Nov 2021
IP
Nov 2021
Biennial Global Immigration Conference
Oct 2021
IP World Summit
Oct 2021
EU Pharmaceutical Regulations & Strategy
Oct 2021
EU Clinical Trial Regulation: Overview and Implementation
Oct 2021
New Medical Device Regulation
Oct 2021
The Role and Skills of a Valuable HR Assistant
Oct 2021
Effective Technology Transfer
Oct 2021
Pharmacovigilance Aspects of Licensing Agreements
Oct 2021
Advanced IVIVC Professional
Sep 2021
Electricity Flexibility, Ancillary Services and Balancing Forum
Sep 2021
Crop Innovations and Regulations
Sep 2021
How to submit variations in Europe MasterClass
Sep 2021
National - Strategy Summit on Paragraph IV Litigation
Sep 2021
ComplianceOnline Medical Device Summit
Aug 2021
MoCannBizCon+EXPO
Aug 2021
National Contract Management Association (NCMA) World Congress
Jul 2021
International Hemp Summit
Jul 2021
AFME/OMFIF European Financial Integration Conference
Jun 2021
World HR Compliance Summit
May 2021
Employment Law in Practice from Recruitment to Termination
May 2021
Fintech & Financing Conference and Expo (FFCON)
May 2021
Required New IT Security at & after Covid19
Apr 2021
Risk Management in Clinical Research
Mar 2021
Probiotics Congress: Asia
Mar 2021
Dark Web Investigation
Mar 2021
Medical Writing Landscape Advancement Summit
Mar 2021
Fraud Analytics
Feb 2021
World Congress on Pharmaceutics, Novel Drug Delivery Systems and Nano Medicine
Feb 2021
International Conference on Computer, Engineering, Law, Education and Management (ICCELEM)
Jan 2021
Stress Testing USA
Nov 2020
Annual Digital Onboarding and ID Verification
Nov 2020
Edition Impact of the Fundamental Review of the Trading Book
Nov 2020
FICO World
Nov 2020
Certified Anti-Corruption Manager® (CACM)
Nov 2020
Public Private Partnership (PPP): Financing, Projects & Contracts
Nov 2020
The International Conference on Clinical Trials and Regulations of Medical Devices and IVD (CSMD)
Nov 2020
EWC European Banking Regulation
Nov 2020
FDA`s Regulation of Regenerative Medicine including Stem Cell Treatments and Tissue Engineering Training
Oct 2020
Validation, Verification and Transfer of Analytical Methods (Understanding and implementing guidelines from FDA/EMA, USP and ICH)
Oct 2020
International Conference on Pharmaceutical GMP, GCP & Regulatory Affairs
Oct 2020
Project Management for FDA-Regulated Companies
Oct 2020
FDA Audit, Quality Assurance Practices, Responsibilities and Expectations
Sep 2020
Chief Litigation Officer Summit Fall
Sep 2020
Virtual ISPOR-FDA Summit
Sep 2020
IFRS 9 Expected Credit Loss Modelling MasterClass
Sep 2020
FDA Boot Camp Boston
Sep 2020
Global CleanTech Summit
Sep 2020
Virtual WFC Money Summit
Sep 2020
International Conference on Law and Political Science (ICLPS)
Sep 2020
Leveraged Lending in the Shifting Economic and Regulatory Environment
Sep 2020
Clinical Trials Inspection Readiness Summit
Aug 2020
Managing Domestic and Foreign FDA Inspections and the COVID-19 Impact
Aug 2020
Life Science Regulatory Information Summit
Aug 2020
Global Conference on Disability and Islam
Aug 2020
The TID Advanced Forum on CFIUS and Foreign Investment Summit
Aug 2020
International Conference on Horizons for Information Architecture, Security and Cloud Intelligent Technology (HIASCIT)
Jul 2020
Emergence of Suicide Bomber
Jul 2020
The International Society for the Advancement of Financial Economics Conference (ISAFE)
Jul 2020
The Arab Pharmacovigilance Guidelines
Jul 2020
Investigational New Drug (IND) & Investigational Device Exemptions (IDE) Applications Preparation and Submission, and Conducting FDA Meetings
Jun 2020
Annual International Conference on Law, Regulations and Public Policy (LRPP)
Jun 2020
Europe Solar + Energy Storage Congress
Jun 2020
Implementing a Bullet Proof Quality System for FDA Audit Success
Jun 2020
FDA`s Ambitious Regulation of Social Media
Jun 2020
Intellectual Property for Pharma Regulatory Affairs
May 2020
Medical Device Regulations in Latin America
May 2020
Airport Security & IT Summit
May 2020
Leading & Developing Successful Pharma Teams
May 2020
Audit Directors` & Managers` Symposium
May 2020
Green Energy Future South Korea
May 2020
Environmental and Public Health Microbiology Conference
May 2020
Oil & Gas Supply Chain Compliance Houston
Apr 2020
The Cosmetic & Beauty Regulations Conference
Apr 2020
Green Energy Future Central Asia
Apr 2020
Mergers and Acquisitions in India: key opportunities and challenges in recent times
Apr 2020
East & Southern Africa Gas & LNG Conference
Apr 2020
Biosimilars
Apr 2020
National Conference of Minority Public Administrators (COMPA) Annual Conference
Mar 2020
Lagos Power Fest
Mar 2020
Construction Law in 8 Hours Masterclass
Mar 2020
Pharmaceutical Regulatory Affairs in Africa
Mar 2020
FDA`s New Import Program for - Strict Precision
Mar 2020
ACES Compliance Summit
Mar 2020
Registration of Veterinary Vaccines in the USA and Canada
Mar 2020
Effective Delegation Skills
Mar 2020
A Practical Approach to Veterinary Vaccine Development and Registration in the EU
Mar 2020
Connectivity in Medical Technology
Feb 2020
Strategic Indirect Tax Directors Forum
Feb 2020
Crisis Negotiation: Managing Critical Incidents Through Effective Negotiation Skills
Feb 2020
Effective Training Skills and Processes in the Pharma Industry
Feb 2020
People Of Determination International Exhibition and Conference (PODIEC)
Feb 2020
EU Medical Device Regulation (MDR) Updated CE Marking Process and ISO 13485: Expectations
Feb 2020
Statistical Analysis of Gages (Metrology)
Feb 2020
FDA Audit Best Practices - Do`s and Don`ts
Feb 2020
Decision Making & Problem Solving in the Pharma Industry
Feb 2020
Innovative Regulatory Pathways Summit
Jan 2020
Anti-Counterfeiting & Brand Protection Summit
Jan 2020
Clinical Trial Regulatory Requirements
Jan 2020
Food Safety & Quality Europe
Jan 2020
Essentials and Overview of the Regulatory Framework in Europe
Jan 2020
Contract and Risk Management for Construction and Capital Project
Jan 2020
Smarter Grants Summit
Jan 2020
Policy Officers’ Intensive
Dec 2019
Regulatory Requirements and Principles for Cleaning Validation
Dec 2019
Annual Summit on Public Consultation and Engagement
Dec 2019
Impact of Brexit on the Pharma & Medical Device Industries
Dec 2019
Advanced Veterinary Pharmacovigilance
Dec 2019
Plastics Regulations US
Dec 2019
The New EU Animal Health Legislation for Veterinary Medicinal Products
Dec 2019
US Patent Practice
Dec 2019
Pharmacovigilance
Dec 2019
How to Write Effective SOPs
Dec 2019
H2020 Master of Finance and Administration and EC Audits
Nov 2019
Edition Impact of SFTR on Securities Lending and Reporting
Nov 2019
MedTech Summit US
Nov 2019
Edition Credit Risk Modeling and Management
Nov 2019
Crime Prevention Through Environmental Design (CPTED)
Nov 2019
API 6D Ball Valves & API 600 Gate Valves
Nov 2019
Pharma IPR USA
Nov 2019
Drafting and Negotiating International Agency and Distribution Agreements
Nov 2019
Annual Update for Senior Trade Mark & Design Administrators
Nov 2019
Horizon Europe: A practical insight
Nov 2019
Applied Statistics for FDA Process Validation
Nov 2019
Global Migration and Wealth Management East Asia
Nov 2019
Managing Your FDA Inspection: Before, During and After
Nov 2019
Confidentiality of Substance Use Disorder Patient Records; Complying with the New Federal Law 42 CFR Part 2
Nov 2019
Pharmaceutical Regulatory Affairs in the Middle East, Dubai
Oct 2019
Predictive Analytics World (PAW) Government
Oct 2019
Drafting Commercial Contracts
Oct 2019
Annual Claims Management & Innovation Conference
Oct 2019
H2020 Fast Track to Financial Rules and Reporting
Oct 2019
BEPS Expert
Oct 2019
Annual Healthcare IT & Digital Health Meeting
Oct 2019
World Congress on Tobacco and Smoking Cessation
Oct 2019
Horizon 2020 Proposal Writing - Focus: Impact
Oct 2019
ISO 13485: Quality Management System for Medical Devices
Sep 2019
Asia Pacific Pharmaceutical and Medical Device Compliance Congress
Sep 2019
Blockchain Confex Vietnam
Sep 2019
Computer System Validation & IT Systems Validation Conference
Sep 2019
Strategic Indirect Tax & VAT Compliance
Sep 2019
International Conference on Anti-Corruption and Integrity (ICOACI)
Sep 2019
Effective Standard Operating Procedure (SOPs) Development
Aug 2019
International Conference on Law, Human Rights, and Cultural Studies (ICLAHS)
Aug 2019
International conference on Public Administration, Policy, and Government (ICPAG)
Aug 2019
Computer System Validation (CSV) and Data Integrity for Clinical Trials Regulated by FDA
Aug 2019
An Introduction to Risk Evaluation & Mitigation Strategies (REMS)
Jul 2019
4-Hour Virtual Seminar on Batch Record Review and Product Release
Jul 2019
HIPAA Privacy Rule Compliance-Understanding New Rules and Responsibilities of Privacy Officer
Jul 2019
21 CFR Part 11 and Risk Assessment
Jul 2019
Death by CAPA Does your CAPA Program need a CAPA
Jul 2019
Workplace Unconscious Bias: Minimizing the Impact on Discrimination, Hiring, Promotions, and Retention
Jul 2019
HEDIS & Quality Improvement Forum
Jul 2019
Advanced Open Source Intelligence (OSINT) for Defence and Security Investigation
Jul 2019
SOPs for FDA-Regulated Industry: Best Practices to Withstand FDA Expectations
Jul 2019
Payments Fraud: Detect & Prevent Check, ACH and P-Card Schemes
Jul 2019
Basics of Testing Associated with Sterilization Validation and Routine Processing
Jul 2019
Process Validation Requirements and Compliance Strategies
Jul 2019
Statistical Process Control - Keys to Prevent Process Variation and Ensure Quality
Jul 2019
Establishing FDA-Compliant Social Media Practices to Avoid FDA Actions
Jul 2019
HIPAA Breach Evaluation and Reporting - What Qualifies as a Reportable Breach and How to Report It
Jul 2019
Pharmacovigilance
Jun 2019
Effective and Pragmatic Vendor Qualification Program for cGMP Compliance
Jun 2019
Dry Powder Inhalers: Annual Conference
Jun 2019
Export Controls & Tech Transfers
Jun 2019
Effective Contamination Control and Environmental Monitoring Program
Jun 2019
FDA Off-Label Promotion Guidelines
Jun 2019
CDR Life Sciences Litigation Symposium
Jun 2019
Strong Customer Authentication Summit
Jun 2019
How to Prepare Yourself for FDA`s on-going Part 11 Inspection Program
Jun 2019
FDA`s Expectations from Supplier Management for GMP: Quality Agreements and More
Jun 2019
Solving Statistical Mysteries – What does the FDA want
Jun 2019
Annual Safety Culture, Leadership & Behavioral Safety
Jun 2019
Equipment Qualification and Process Validation
Jun 2019
FDA`s 21 CFR Part 11 Add-on Inspections
Jun 2019
CAPA Simplified - A one-form, easy-to-complete, method for simplifying your CAPA Process
Jun 2019
Best Practices to Obtain FDA Feedback Prior to 510(k) and De Novo
Jun 2019
Cross-border Fintech: Regulation and the Law
Jun 2019
Risk Analysis and HACCP
Jun 2019
Anti-Money Laundering Compliance for Law Firms
May 2019
Mindfulness in the Workplace
May 2019
BSA/AML Contextual Awareness of High Risk Customers
May 2019
Structuring and Auditing Physician Medical Director and Administrative Arrangements: Key Stark Law Considerations
May 2019
3-Hour Virtual Seminar on Qualification (IQ, OQ, PQ) and Validation of Laboratory Equipment and Systems for Regulated Industries
May 2019
HIPAA Compliance Monitoring and Auditing
May 2019
Overcoming Obstacles of the Canadian Drug Regulatory Landscape
May 2019
International Conference on Food Safety and Regulatory Measures
May 2019
Annual ISO 26262- Automotive Functional Safety Forum
May 2019
FDA Expectations for 505(b)(2) Regulatory Pathway for New Drugs
May 2019
Exploring the FDA Refuse-To-Accept (RTA) Guidance for 510(k) Submissions
May 2019
Supplier Quality Assurance Agreements: Why a General Supply Agreement Not Be Enough with Some Suppliers
May 2019
Optimising the Back Office Function in Energy and Commodity Trading
May 2019
Cyprus IT Forum (CIF)
May 2019
FDA Recalls - Before You Start, and After You Finish
May 2019
Statistical Techniques for Medical Device Manufacturers
May 2019
Texting and Mobile Devices in Healthcare - HIPAA and CMS Requirements for Security of PHI
May 2019
Aviation Quality & Safety Management in an EASA Environment Symposium
May 2019
VA Healthcare
May 2019
ISO 26262 USA
May 2019
Label Claims for food, Probiotics and Cosmetic products in Brazilian Regulatory System
May 2019
How to Ensure Your Foreign Vendors are FDA Compliant: Conducting Vendor Audits, Monitoring, and Using Checklists
May 2019
ISO 62304 How to Create a Medical Software Development File?
May 2019
3-Hour Virtual Seminar on Best Practices to Help you Pass an FDA Computer System Validation Audit
May 2019
Exploring Routes to Market for Herbals
May 2019
Excel Spreadsheets: Develop and Validate for 21 CFR Part 11 Compliance
May 2019
Legal Issues Concerning Employees with Psychiatric Illness
May 2019
How to Properly Manage a Regulatory Inspection
May 2019
The Requirements and Responsibilities of a HIPAA Security/Privacy Officer
May 2019
FDA Rules for Pharmaceutical Analytical Method Validation
May 2019
Annual Practical CVA and KVA Forum
Apr 2019
International Congress on New Horizons in Education and Social Sciences (ICES)
Apr 2019
Global Blockchain Summit Slovenia (Rescheduled to a later date)
Apr 2019
In-Depth Testing of Computer Systems Regulated by FDA
Apr 2019
API International Trade and Customs Conference
Apr 2019
Essentials of Validation - IQ, OQ, PQ
Apr 2019
FDA and EU Process Validation and Equipment Qualification
Apr 2019
Ensuring your Site is Ready for an FDA Inspection
Apr 2019
Continued Process Verification - A Systematic Approach
Apr 2019
The Healthcare Quality Improvement Act: Achieving Immunity in Your Peer Review Process
Apr 2019
ANDA Submission and GDUFA Final FDA Guidance
Apr 2019
Investigational New Drug (IND) & Investigational Device Exemptions (IDE) Applications Preparation and Submission, and Conducting FDA Meetings
Apr 2019
Medical Device Laws and Regulations in Asia - Part 2 - India, Japan, and Korea
Apr 2019
Data Integrity: Compliance with 21 CFR Part 11, SaaS-Cloud, EU GDPR
Apr 2019
FDA Regulations & New Legislation for Marketing Cosmetics in the U.S
Apr 2019
FDA`s New Import Program for
Apr 2019
Loan Documentation
Apr 2019
Horizon 2020 Financial Rules and Reporting
Apr 2019
510(k) and PMA Refuse to Accept Policy
Apr 2019
Oklahoma’s Industrial Cannabis Expo
Apr 2019
Medical Device Laws and Regulations in Asia – Part 1 – China
Apr 2019
Medical Device Laws and Regulations in Asia – 2 Part Web-Series
Apr 2019
Supply Chain Traceability is Going Digital: What Can You do to be Prepared
Apr 2019
In Depth Testing of Computer Systems Regulated by FDA
Apr 2019
FDA Regulations for Pharmaceutical Current Good Manufacturing Practice (cGMP)
Apr 2019
Edition Nordic Asset Allocation: Investing in Alternative Asset Classes
Mar 2019
Biosimilars and Follow-On Biologics Americas
Mar 2019
Verification, Validation and Compliance for Medical Device Software
Mar 2019
Harmonized Tariff Schedule Classification
Mar 2019
Cyber Security for Critical Infrastructure
Mar 2019
Pre-Filled Syringes
Mar 2019
Insider Threat Management
Mar 2019
FDA Inspections - Do`s and Don`ts
Mar 2019
Device Changes, FDA Changes, and the 510(k)
Mar 2019
The DIOM – A Straightforward Method for Meeting FDA Requirements for Design Inputs and Outputs
Mar 2019
EU and US GMP/GDP – Similarities and Differences
Mar 2019
FDA Regulation of Over-the-Counter (OTC) Drugs
Mar 2019
Zero Acceptance Sampling to Reduce Inspection Costs
Mar 2019
FDA`s Quality Metrics - Latest Advances
Mar 2019
Selection and Use of (Certified) Reference Material in Analytical Laboratories
Mar 2019
FDA’s New Enforcement of 21 CFR Part 11
Mar 2019
CMO Supplier Quality Agreements - How to Comply with New FDA and EU Guidelines for Contract Drug Manufacturers
Mar 2019
The Most Serious FDA 483s - How to Avoid Them
Mar 2019
3-Hour Virtual Seminar on FDA`s Scrutiny of Social Media Promotion
Mar 2019
FDA`s Scrutiny of Social Media Promotion
Mar 2019
Patient Rights, Medical Records and HIPAA - What You Need to Know as a Healthcare Provider
Mar 2019
The Global Citizenship and Residency Summit
Mar 2019
The FDA Inspection: Preparation, Management, and Follow - up
Mar 2019
Good Documentation Practices to Support FDA Computer System Validation
Mar 2019
SOP Writing, Training and Compliance in the Pharmaceutical Industry
Mar 2019
CMO Supplier Quality Agreements – How to Comply with New FDA and EU Guidelines for Contract Drug Manufacture
Mar 2019
Criminal Background Checks in the Hiring Process
Mar 2019
Pharmacovigilance / GCP Audit Report Writing
Mar 2019
FDA Regulations for Environmental Monitoring (EM) Program
Mar 2019
The New ICH GCP E6 R2 Guideline
Feb 2019
Mortgage Servicing Compliance: Meeting Extensive New Regulatory Expectations
Feb 2019
New Crystalline Silica Requirements and Strategies
Feb 2019
Form 941 for : All You Need to Know
Feb 2019
GDPR and Implications on Drug Development
Feb 2019
Introduction to Root Cause Investigation for CAPA
Feb 2019
Measurement Systems Analysis
Feb 2019
Europe Conference: Embracing Change
Feb 2019
Surviving an FDA Sponsor Inspection - Training for Success
Feb 2019
Complaint Handling Best Practices - Compliance with FDA and ISO Regulations
Feb 2019
USP [1224] Transferring the Method to meet Regulatory Expectations
Feb 2019
REACH Practicalities MasterClass
Feb 2019
Compliance Risk Management in Medical Devices, Pharmaceuticals, and Combination Products
Feb 2019
The SEC`s New Whistleblower Rules: Implications for Your Company`s Compliance and Fraud Program
Feb 2019
What FDA-Regulated Industry Should Know about FDA’s New Policy on GMP Enforcement
Jan 2019
In-Depth Computer System Validation (CSV) for FDA Compliance
Jan 2019
Step-by-Step Internal Investigations Best Practices
Jan 2019
Medical Device Cybersecurity and FDA Compliance
Jan 2019
If it Isn`t Written Down, then it Didn`t Happen: Complying with FDA`s Good Documentation Practices
Jan 2019
Data Governance for Computer Systems Regulated by FDA
Jan 2019
Healthcare Privacy and Security Regulations: Satisfying HIPAA, GDPR, 42 CFR Part 2, FERPA, and State Laws Protecting Health Information
Jan 2019
How to prepare an Effective Audit Manual for an Internal Audit Department
Jan 2019
AML Model Validation: A Critical Need in the New Regulatory Environment
Jan 2019
How to Prepare for an FDA Inspections?
Jan 2019
Medical Marijuana in the Workplace
Jan 2019
Strategies for Mitigating the Impact of China Tariffs
Jan 2019
Nuclear Power Plant Life Management & Extension
Dec 2018
Preparing to Comply with the New FDA FSMA Rules: Planning Valid Preventive Food Safety Controls
Dec 2018
The Borderline Between Medicines and Foods
Dec 2018
Payroll in the Complicated States of California, New York, and Pennsylvania
Dec 2018
Pacing Delay - The Practical Effect on Projects and Delay Claims
Dec 2018
In a Nutshell: Data Protection & Privacy Legislation in the U.S. & European Union
Dec 2018
Handling Situations Where Regulation E and ACH Don`t Align
Dec 2018
FDA Regulations for Analytical Instrument Qualification and Validation – Comprehensive Best Practices
Dec 2018
The Life Cycle Approach to Cleaning Validation
Dec 2018
Tougher Import Rules for FDA Imports in
Dec 2018
GDPR Update for Global Organization
Dec 2018
Conducting Effective Investigations of Out of Specification and Atypical Laboratory Results
Dec 2018
How to be efficient and compliant with 21 CFR Part 11, data integrity, SaaS/Cloud, and EU GDPR
Dec 2018
Title IX Coordinator Training and Certification: Leading Your Institution’s Efforts
Dec 2018
Edition Fair and Prudent Valuation for Derivatives
Nov 2018
Master Class in Interconnection and Next Generation Networks and Access (TRMC)
Nov 2018
Edition Capital Raising Instruments under TLAC and MREL
Nov 2018
Saudi Arabia Renewable Energy - Solar & Wind
Nov 2018
H2020 Master of Finance and Administration
Nov 2018
Edition of Managing Interest Rate Risk Arising from Non-Trading Book Activities
Nov 2018
ICA’s inaugural Asia Pacific conference: The BIG Compliance Conversation
Nov 2018
Managing Practical Behavior Based EHS Programs
Nov 2018
Developing and Implementing a Global Regulatory Plan and Strategy
Nov 2018
The Africa Renewable Energy Forum
Nov 2018
Medical Records: Compliance with CMS Hospital CoPs and Proposed Changes
Nov 2018
Good Documentation and Record Keeping Best Practices (FDA & EMA)
Nov 2018
Construction Law in 8 hours Masterclass
Nov 2018
Customs Compliance in Europe
Nov 2018
Ensuring Integrity and Security of Laboratory Data
Nov 2018
Data Integrity in the Pharmaceutical Industry
Nov 2018
Development of Drug/Device and Device/Drug Combination Products
Nov 2018
The International Conference on Cyber Security, Cyber Welfare, and Digital Forensic (CyberSec)
Oct 2018
Developing an Assistance Animal Compliance Policy
Oct 2018
How to Perform a HIPAA Risk Assessment and Write Policies
Oct 2018
Watec Italy - Water Technology and Environmental Control Exhibition & Conference
Oct 2018
Japan: Regulatory Compliance Requirements for Life Science Products
Oct 2018
Uncovering and Managing Successful Post Market Compliance for Medical Devices
Oct 2018
Conflict Management
Oct 2018
World Litigation Forum USA
Oct 2018
Workplace Violence Prevention Programs Including Active Shooter Scenarios
Oct 2018
FDA’s Adverse Event Reporting and Product Recalls
Oct 2018
SOP Writing, Training and Compliance in the Pharmaceutical Industry
Oct 2018
21 CFR Part 11 Compliance for Computer Systems Regulated by FDA
Oct 2018
H2020 Proposal Writing Academy + Marie Sk odowska-Curie (ITN/ETN) Proposal Writing
Oct 2018
Marie Sklodowska-Curie (ITN/ETN) Proposal writing
Oct 2018
Horizon 2020 Proposal Writing Academy
Oct 2018
Managing Construction Suspension and Contract Termination Masterclass
Oct 2018
Effective Batch Record Review
Oct 2018
Developing Effective Compliant Documentation and Training System
Oct 2018
FDA`s New Draft Guidance on Software and Device Changes and the 510(k)
Oct 2018
Secrets to Writing Effective SOPs for Medical Device QMS
Oct 2018
Medical Device Hazard Analysis Following ISO 14971
Oct 2018
Powerful Closed-loop CAPA - Meeting FDA Expectations
Oct 2018
FDA Auditing Practices and the Top 10 Most Common Cited GMP Deficiencies
Oct 2018
Annual Capital Adequacy and Stress Testing
Sep 2018
Annual Best Execution and Transparency under MiFID II
Sep 2018
Anti-Counterfeiting & Brand Protection Summit
Sep 2018
Preparation for FDA and EU Regulatory Inspections
Sep 2018
How FDA Trains Its Investigators and Inspectors to Review Sub-Systems for State of Compliance: What You Need to Do to Prepare for a Successful Inspection
Sep 2018
Recent FDA Auditing Practices and the Top 10 Most Common Cited GMP Deficiencies
Sep 2018
Edition Insurance ALM and Asset Allocation under Solvency II
Sep 2018
Hosting FDA Regulatory Inspections
Sep 2018
European Prefilled Syringes Summit
Sep 2018
Writing Effective Analytical Procedures
Sep 2018
FDA`s New Enforcement of 21 CFR Part 11
Sep 2018
The Legal AI Forum
Sep 2018
System Suitability Testing (SST) for USP and FDA Compliance
Sep 2018
Annual Subprime Credit Forum
Sep 2018
Chipping away at constraints – Practical tips to Improve your Manufacturing Operations
Sep 2018
Mining Law in 8 Hours Masterclass
Sep 2018
How to be efficient and compliant with 21 CFR Part 11, data integrity, and SaaSCloud
Sep 2018
FDA`s Revolutionary Change in Software Regulation
Aug 2018
How To Perform High Quality Safety Investigations
Aug 2018
Pharmaceutical Validation - Latest Global Regulations and Trends to Stay Compliant
Aug 2018
HIPAA Training for Compliance Officer
Aug 2018
APS 5-6 Communication Professionals Leadership Workshop
Aug 2018
Understanding the HIPAA Compliance Requirements
Aug 2018
HIPAA Breach Evaluation and Reporting - What Qualifies as a Reportable Breach and how to Report It
Aug 2018
What do the FDA, EMA and PMDA Look for When Conducting cGMP Regulatory Inspections
Aug 2018
EL1 & EL2 High Performance and Leadership Workshop
Aug 2018
National Small Business Federal Contracting Summit- Summer
Aug 2018
The Role of the HIPAA Security Official
Aug 2018
Design Control Basics
Aug 2018
Deciding When to Submit a 510(k) for a Change to an Existing Device
Aug 2018
Microsoft Excel - Let`s Look Beyond the Look-Up
Aug 2018
FDA Compliant QC and QA Practices – Creating a Perfect, Audit-Ready QMS
Aug 2018
Building a Compliant Documentation and Training System
Aug 2018
Seminar on HIPAA and Beyond
Aug 2018
Public Sector Women’s Leadership Workshop
Jul 2018
Developing a Contractor Safety Program
Jul 2018
Sunshine Act Reporting: Clarification for Clinical Research
Jul 2018
Accelerating ISO 55000 Compliance for Integrated Asset Management
Jul 2018
Japan - Regulatory Filing Requirements and Compliance Processes for Life Sciences
Jul 2018
How to Make Sure Your Foreign Vendors are FDA Compliant and Stay that Way
Jul 2018
The International Search & Rescue Conferences & Exhibition
Jul 2018
Practical Risk Appetite and Risk Tolerance
Jul 2018
Patients Suing Under HIPAA
Jul 2018
Agile, Testing and DevOps Showcase
Jul 2018
California Water Summit
Jun 2018
Policy Professionals Leadership Workshop
Jun 2018
National Policy Officers Conference
Jun 2018
The Contingency Contracting Summit (C2)
Jun 2018
Webit.Festival Europe
Jun 2018
Food Fraud in the Organic Industry
Jun 2018
Trade Compliance Seminar - Harmonized Tariff Schedule/Schedule B and NAFTA Rules of Origin and Documentation
Jun 2018
Implementing Bank Secrecy Act (BSA), Audit & Best Practices
Jun 2018
Things you need to know about information governance to sell healthtech products into the NHS
Jun 2018
Public Sector Women in Leadership Workshop
Jun 2018
How to prepare for a CBP Audit
Jun 2018
Oversight of CROs-Vendors-CMOs
Jun 2018
Europe`s Commodity Trade Finance Forum
Jun 2018
Corrective and Preventive Action (CAPA) per FDA Requirements
Jun 2018
Pricing Interest Rate Derivatives
Jun 2018
Off label Promotion of Drugs and Medical Devices - FDA`s Latest
Jun 2018
Environmental Compliance and Safety Management Inspection and Audit Techniques
May 2018
Governance and Change Control According to GxP/GMP Requirements
May 2018
Form W-2 for : All You Need to Know
May 2018
Pharma Cold Chain Summit
May 2018
Minimising Corruption, Fraud And Misconduct
May 2018
Export Documentation and Procedure
May 2018
Employee Retention Toolkit : Set the Stage to meet Employee Expectation - Module 2
May 2018
Product Recalls Forum
May 2018
The New EU Medical Device regulation
May 2018
Investigator Reporting Responsibilities: AEs, Unanticipated Problems, Modifications, and Deviations
May 2018
Full Spectrum Air Defence Asia
May 2018
GMP Expectations for Products Used in Early Phase IND Studies
May 2018
Combination Products Regulations: Drug and Device Combinations in the USA and EU
May 2018
Health Product Marketing authorization in Brazil - Documentation, Approval Process, Labeling, Advertising and Post Market Vigilance
May 2018
Employers Guide to HIPAA
May 2018
New Hire Legal Requirements and Process
May 2018
Different requirements for Phase I Investigational Drug Products:
May 2018
International Conference on Bioethics in the New Age of Science (BNAS)
May 2018
EuroCyber
May 2018
Chief Medical Officer Summit
May 2018
Validation and 21 CFR Part 11 Compliance of Computer Systemse
May 2018
Excellence in Claims Management
May 2018
HIPAA Security and Beyond
May 2018
Auditing Analytical Laboratories for FDA Compliance
May 2018
How to Comply with 21 CFR 11 Requirements for Electronic Medical Records
May 2018
The Annual European Renewable Energy Investors Council
Apr 2018
Annual Global Pharma Regulatory Summit India
Apr 2018
Statistical Sampling Plans - Methods and Applications
Apr 2018
Managing Your FDA Inspection: Before, During and After
Apr 2018
Operational and Technical Implementation of IFRS 16
Apr 2018
Public Sector Tier 4, 5 & 6 Leadership Success Workshop
Apr 2018
Annual Behavioral Safety & Culture: Barriers & Success Stories
Apr 2018
Women in Listed Companies Leadership Summit
Apr 2018
Preparing the Marketing Authorization Application in the EU, with a focus on the product information
Apr 2018
Responding to the Opioid ​Crisis: Litigation, Regulation & Reform
Apr 2018
The Use of Drug Master Files & Quality Agreements: Understanding and Meeting your Regulatory and Processing Responsibilities
Apr 2018
Differences Between ISO 13485 & ISO 9001 - and How to Choose Which One to Implement
Apr 2018
eCTD Submissions of IND/NDA to the US FDA, EU and Canada
Apr 2018
A Risk Based Strategy for the Development & Validation of and Validation of Analytical Methods with a QbD Approach
Apr 2018
Quality Management and Quality Audit According to Gxp-GMP Requirements
Apr 2018
HIPAA Risk Analysis: Clarified, Explained, Demonstrated
Apr 2018
Annual Pharmacovigilance Forum
Mar 2018
FDA Penalties for Regulatory Non-Compliance in the Pharmaceuticals Industry
Mar 2018
European Data Protection Regulation - Implementation
Mar 2018
Integrated Strategic Financial Management for the Public Sector Workshop
Mar 2018
Pre-Filled Syringes
Mar 2018
HIPAA Compliance - What you Need to Know
Mar 2018
Dietary Supplements CGMPS - 21 CFR 111 Compliance
Mar 2018
Eliminating Microbial Contamination in a Spiral Freezer
Mar 2018
HIPAA Compliance
Mar 2018
Essentials of Dealing with Non-Conforming Material
Mar 2018
Bioavailability and Bioequivalence Studies Submitted in NDAs and INDs for Orally-Administered Drug Products
Feb 2018
Refining Regulation to Strengthen Compliance
Feb 2018
Corporate Compliance & Transparency in Pharma Summit
Feb 2018
GMP for Quality Control Laboratories and FDA Audit Preparation
Feb 2018
Fundraising Under HIPAA: What You Need to Know, What You Need to Do
Feb 2018
Acceptance Activities in FDA QSR
Feb 2018
HIPAA Changes : How to Comply
Feb 2018
Validation of FDA-Regulated Computer Systems
Feb 2018
International Conference on Government, Law and Culture (ICGLC)
Jan 2018
Cyber Security & Data Privacy and Protection
Jan 2018
Consumer Finance Class Actions & Litigation
Jan 2018
Advancing Construction Claims
Jan 2018
Risk Based Project Management for the Life Sciences Industry
Jan 2018
Biometrics Israel
Jan 2018
Validation and 21 CFR Part 11 Compliance of Computer Systemst
Jan 2018
Compensation-Focused Compliance: Is Your Healthcare Organization Ready for Shifts in Stark Law Enforcement?
Dec 2017
Consumer Identity World APAC
Dec 2017
Validation and Use of Excel Spreadsheets in FDA Regulated Environments
Dec 2017
FDA Regulation of Dietary Supplements
Dec 2017
HIPAA - How Business Associates Can Comply Calmly, Confidently and Completely
Dec 2017
FDA`s Latest Regulations for Computer Systems Used in the Tobacco and Related Industries, Effective 08/08/2016
Dec 2017
Applied Statistics, with Emphasis on Risk Management in R&D, QA/QC, and Manufacturing
Dec 2017
Gas Trading & Infrastructure Forum
Nov 2017
Human Subjects Research Seminar: Current Regulations under FDA and HIPAA
Nov 2017
Pharmaceutical Regulatory Affairs in Latin America
Nov 2017
Annual Operational Risk Management in the Digital Age
Nov 2017
Port & Terminal Concessioning Course
Nov 2017
New Approaches to Legislative Reform
Nov 2017
DIA Middle East Regulatory Conference
Nov 2017
Port Finance International London Conference
Nov 2017
Compliance Boot Camp
Nov 2017
Global Compliance and Anti Corruption Summit
Nov 2017
FDA`s Latest Regulations for Tobacco Industry Effective 8-2016
Nov 2017
GMP and Regulatory Expectations for Early IND Products
Nov 2017
POPI vs Cyber Security
Nov 2017
Medical Device Hazard Analysis Following ISO 14971
Nov 2017
New Cosmetic Product Regulation in World Economies
Nov 2017
e-Discovery & e-Investigations Forum
Oct 2017
Biometrics
Oct 2017
I-9 and Immigration Enforcement Bootcamp: Employer Best Practices & Compliance
Oct 2017
Complaints, Adverse Event Reporting, and Recalls - An Integrated Approach
Oct 2017
InvestPro Kazakhstan Almaty
Oct 2017
Validation, Verification and Transfer of Analytical Methods from FDA/EMA, USP and ICH
Oct 2017
Managing Your FDA '483' Inspectional Observations
Oct 2017
The Regulations of OTC Drugs
Oct 2017
How TGA, FDA & Other Regulatory Authorities Inspect Computerized Systems for Data Integrity
Oct 2017
Navigating the Maze for Post-Market Compliance -- Complaint Handling, MDRs, Recalls and Proposed Guidance on FDA Risk Benefits
Oct 2017
African Ports Evolution
Oct 2017
FDA Regulations for Analytical Instrument Qualification and Validation Processes
Oct 2017
Japan - Regulatory Filing Requirements and Compliance Processes for Medical Devices
Oct 2017
HIPAA Changes for and Beyond
Oct 2017
Australian Regulatory Guidelines for Medical Devices (ARGMD): Government Reimbursement, Requirements, Fees and Turnaround Time to Product Approval
Oct 2017
Validation, Verification and Transfer of Analytical Methods (Understanding and implementing guidelines from FDA/EMA, USP and ICH)
Oct 2017
The Development and Implementation of a Robust Food Safety, Defense and Quality Assurance System
Oct 2017
FDA`s Latest Regulations for Computer Systems Used in the Tobacco
Oct 2017
GLP Quality System Essences and Comparison with GMP
Oct 2017
Pharmaceutical Quality Management System (GMP Requirements, ICH Guidance, QbD, and USFDA/EMA Regulations)
Oct 2017
Practical Issues for Trading the Next Generation of ETFs
Sep 2017
IoD Hertfordshire - Data Protection. Are you prepared for the GDPR?
Sep 2017
FDA Scrutiny of Promotion and Advertising Practices
Sep 2017
Insurance ALM and Asset Allocation under Solvency II
Sep 2017
Title IX Training Bundle: Presidents and Study Abroad
Sep 2017
ISO 13485, ISO 14971, Quality Document Management, and Risk Management for Medical Devices
Sep 2017
The A to Z of Trade Compliance for a U.S. Entity
Sep 2017
Effective Training Practices for FDA Compliance
Sep 2017
FDA`s Import Program for - New Pathways and Pitfalls
Sep 2017
Edition Risk Audit in Banking
Sep 2017
Law Enforcement Risk Management Summit
Sep 2017
Essentials of Validation -IQ,OQ,PQ
Sep 2017
The EU General Data Protection Regulation (GDPR)
Sep 2017
Investigation of Out-Of-Specification Laboratory Results
Sep 2017
Medical Ethics and Legal Medicine
Sep 2017
FEM APAC Global Mobility Summit & EMMAs
Sep 2017
Job-Specific BSA for Deposit Operations: SAR Monitoring, 314(a) Requests & CIP
Sep 2017
Annual Credit Law Symposium
Sep 2017
Stress-Testing for Financial Institutions, Beyond Regulatory Constraints
Sep 2017
Menu Labelling: Knowing the Requirements and Available Options to Achieve Compliance
Sep 2017
Data Integrity and Its Issues
Sep 2017
Annual Pharmaceutical Compliance in Latin America Congress
Aug 2017
Social Security - What Advisors Need to Understand Regarding Social Security When Meeting With Clients
Aug 2017
Navigating the Financial Regulations of Cybersecurity
Aug 2017
Nonresident Alien Vendors – How To Handle The Information Reporting And Backup Withholding Requirements Of The IRS
Aug 2017
Child-Centred Approaches to Ending Family Violence Melbourne
Aug 2017
European Regulatory Procedures - Comprehensive Overview of EMA and National Requirements and other Agencies
Aug 2017
CRE Collateral Valuation Process: Conducting a Risk Assessment
Aug 2017
FDA`s Medical Device Clinical Trials Program
Aug 2017
New FDA FSMA Rules on the Sanitary Transportation of Human and Animal Foods
Aug 2017
CMS Revised Hospital CoP Dietary, CAH Dietary, DNV Healthcare and TJC Standards
Aug 2017
Documenting Software for FDA Submissions
Aug 2017
FDA Regulations for Environmental Monitoring (EM) Program
Aug 2017
How to Prepare for and Host a FDA Inspection and Respond to 483`s
Aug 2017
Building a Validation Program From Top to Bottom
Aug 2017
FDA Legal Writing Skills that Result in Effective Regulatory & Quality Submissions
Aug 2017
Validation and 22 CFR 11 Compliance of Computer Systems Intermediate to Advanced
Jul 2017
Compliance Secrets from a Former Customs Officer
Jul 2017
Pharmaceutical Quality Risk Management (QRM) Overview
Jul 2017
Power Purchase Agreement - Kuala Lumpur
Jul 2017
Innovating for Better Regulatory Outcomes Canberra
Jul 2017
A Comprehensive View of FDA Regulations for Medical Devices
Jul 2017
HUD Affirmatively Furthering Fair Housing Rule: Compliance for Governments
Jul 2017
Quality Management Systems that Comply with ISO13485: 2016
Jul 2017
World CDx: Market Access for Precision Medicine
Jul 2017
FERPA for Faculty
Jul 2017
Law Enforcement Opioid Response Forum
Jul 2017
Personnel Training to Assure FDA and ISO Compliance
Jul 2017
Modern HIPAA Compliance - Managing Privacy, Security, and Breach Notification in a World of New Technologies, New Threats, and New Rules
Jul 2017
FDA`s Regulation of Regenerative Medicine including Stem Cell Treatments, Tissue Engineering and Gene Therapies
Jul 2017
Understanding the FDA`s Regulation of HCT/Ps and Successful Product Development Strategies
Jul 2017
FERPA Hot Topics: Big Challenges Solved
Jul 2017
Applying the FDA Food Safety Modernization Act (FSMA) to Your Organization: 2-day In-person Seminar
Jul 2017
Implementing Agile in an FDA-Regulated Environment
Jul 2017
Mastering U.S. Export Administration Regulations
Jul 2017
Combination Products Registration
Jul 2017
USFDA Food Import and Export: Current and Future Safety Regulations
Jul 2017
Dealing with Disability-A Medical/Legal Approach
Jun 2017
Understanding Federal Government Payments
Jun 2017
Mastering HTSUS and Schedule B Code Classifications
Jun 2017
FEM Global Mobility Conference Sydney
Jun 2017
Water Market Reform
Jun 2017
Negotiating and Mediating Health Care Disputes
Jun 2017
Baltic Geodetic Congress (Geomatics)
Jun 2017
Overview of Device Regulation - FDA
Jun 2017
OSHA 29 CFR 1910.95 - Best Practices in Implementing a Successful Hearing Conservation Program
Jun 2017
What Every Employer Needs to Know about Proposed Immigration Changes in the Trump Era
Jun 2017
` -Parties - Who are They, How To Identify Which -Party They Are, and What Are Their Responsibilities in the ACH Network?`
Jun 2017
New England Municipal Finance Summit
Jun 2017
FDA Requirements for the Pharmaceutical Industry: Inspection, OTC Drugs, IND/NDA/ANDA, eCTD and GMP Requirements
Jun 2017
Mastering Treasury`s New Customer Due Diligence Final Rule
Jun 2017
Texting and E-mail with Patients — Meeting Patient Desires According to the Rules
Jun 2017
How to Manage the HIPAA Business Associate Process
Jun 2017
Harbottle and Lewis GDPR Tech Roundtable
Jun 2017
Annual America`s Small Business Summit
Jun 2017
Cosmetics Product Regulation - Four Years after its implementation
Jun 2017
Dealing with the Weingarten Ruling (Interviewing Public Sector and Private Sector Union Employees)
Jun 2017
FDA Policy and Goals Regarding the 483 Response
Jun 2017
Addressing The BREXIT Challenge
Jun 2017
Document Retention and Destruction What Human Resource Professionals Must Know
May 2017
Applying U.S. FDA Laws and Regulations to Each Phase of Total Product Life Cycle (TPLC)
May 2017
Annual MiFID II for Energy and Commodity Firms
May 2017
Brazil Summit on Anti-Corruption
May 2017
Intelligence Analytics Summit
May 2017
How to Conduct a HIPAA Risk Assessment
May 2017
Claims Adjustment Reason Codes 'CARC' and Remittance Advice Remark Codes 'RARC' Impact - How to Effectively Manage Denials
May 2017
Managing a Union Represented Workplace
May 2017
Efficient Process Validation Strategies and Validation Master Plan (VMPs) for Medical Devices
May 2017
Roadmap to Advanced Human Resources and Employment Law
May 2017
New FDA or EMA and USP Guidelines for Transfer of Analytical Methods
May 2017
Employment-at-Will! Does It Protect Employers from Wrongful Termination Allegations?
May 2017
The Housing Delivery In Practice Conference
May 2017
How to Prepare for a Customs Focused Assessment Audit and Self Audit your Import Program
May 2017
BIGIT GOV
May 2017
Phase I GMPs
May 2017
FDA Scrutiny of Promotion and Advertising Practices
May 2017
Operational and Technical Challenges for PRIIPs
May 2017
Export Control Recordkeeping and Compliance Automation
May 2017
Market Developments within Direct Lending
May 2017
Extractables & Leachables USA
May 2017
Use of Electronic Health Record Data (EHR) in FDA regulated clinical investigations
May 2017
Sales and Use Tax - Best Practices
May 2017
Modern HIPAA Compliance - Managing Privacy, Security, and Breach Notification in a World of New Technologies, New Threats, and New Rules
May 2017
HIPAA Compliance
May 2017
Annual Focus Event on Registrant Regulation Conduct & Compliance
May 2017
Cosmetic Regulations in Major World Economies (EU, USA, Brazil, China, Japan, Korea, ASEAN)
May 2017
Preparing Compliant eCTD Submissions
Apr 2017
Innovation and Global Issues in Social Sciences
Apr 2017
Government IT Modernization
Apr 2017
Preparing Premarket Submissions that secures U.S. FDA Clearances/Approvals: 510(k)/Pre-IDE/IDE and PMA
Apr 2017
The International Conference on Landmine: Detection, Clearance and Legislations (LDCL2017)
Apr 2017
Best Practices for Preparation for, Behavior during, and Response to an FDA Inspection
Apr 2017
CIBSE BIM Roadshow: Newcastle
Apr 2017
GxP (GMP, GLP, GDP) Data Integrity, Quality Metrics and FDA Inspections
Apr 2017
ISO 13485:2016 Utilizing Lean Documents and Lean Configuration
Apr 2017
GlobalCompliancePanel is conducting a seminar on FDA Data Integrity for Computerized Systems
Apr 2017
Understanding and Implementing USP 1058 Analytical Instrument Qualification
Apr 2017
Thriving with the Revised ISO 14001 Standard; Key Changes and Transition Strategies
Apr 2017
FERPA for Advancement: Train Your Whole Shop
Apr 2017
Annual Medicaid Managed Care Leadership Summit
Apr 2017
New HIPAA Audit and Enforcement Activities: Being Prepared to Show your Compliance
Apr 2017
What You Should Know About Export Requirements for FDA Regulated Products from the US to Foreign Countries
Apr 2017
Preparing a US FDA Medical Device 510(k) Submission and Deciding When to Submit a 510(k) for a Change to an Existing Device
Apr 2017
MDTI - Medical Device School
Apr 2017
Digital Regulation Forum
Apr 2017
New GS1 US Guideline - Pharmaceutical Industry Prepares for DSCSA Item-Level Traceability Requirements
Apr 2017
Compliance with Laws Governing Pregnant Employees and New Parents: Pregnancy at Work
Apr 2017
Identifying, Reporting and Monitoring Suspicious Activity (SAR)
Apr 2017
Preparation for GMP Inspections by Regulatory Agencies
Apr 2017
The Commonwealth and challenges to media freedom
Apr 2017
Pharmaceutical and Biologics Facility Design: FDA and Regulatory Aspects
Apr 2017
Annual Russian Retail Forum
Mar 2017
How to Detect & Prevent Expense Reimbursement Fraud and Protect Your Organization
Mar 2017
Mozambique Corporate Social Responsibility Conference & Exhibition
Mar 2017
The 10 Step HIPAA Compliance Review
Mar 2017
FDA & CFIA 2016 Regulatory Changes/Updates
Mar 2017
Telehealth: Understanding JCAHO Standards and Legal Regulatory Compliance
Mar 2017
Active Shooter Training: Preparing Your Faculty and Staff
Mar 2017
Managing an FDA Inspection
Mar 2017
Healthcare Biometrics Summit
Mar 2017
CIBSE BIM Roadshow: Dublin
Mar 2017
CIBSE BIM Roadshow: Belfast
Mar 2017
Intermediate Title IX Institute and Certification
Mar 2017
Ransomware and HIPAA Risks - Be Very Careful Here
Mar 2017
Title IX: Four Essentials for Faculty
Mar 2017
Urology Joint Advocacy Conference
Mar 2017
HIPAA Changes
Mar 2017
HIPAA Compliance Virtual Boot Camp
Mar 2017
CIBSE BIM Roadshow: Edinburgh
Mar 2017
IBESRA (International Business Economics Social Sciences Research Association) Conference
Feb 2017
Trial Master File (TMF): FDA Expectations from Sponsors and Sites
Feb 2017
Outsourcing and Vendor Management in Financial Institutions
Feb 2017
Microsoft Excel Series - Part 3: Beyond IF and Excel Macros
Feb 2017
CIBSE BIM Roadshow: Bristol
Feb 2017
Complying with `Made in USA` Labeling Standards
Feb 2017
Managing Risk in Africa
Feb 2017
Preparing Form 1040NR: U.S. Nonresident Alien Income Tax Return
Feb 2017
European Consumer Protection Conference
Feb 2017
National Working with Men to Tackle Family Violence
Feb 2017
CUSTOMS VALUATION: How to Determine the Customs Value - Part 1
Feb 2017
Body-Worn Camera Winter Forum
Feb 2017
HIPAA Challenges in Email and SMS Communication
Feb 2017
EE0-1 Reporting Form Changes in and How Company`s Can Be Compliant
Feb 2017
The HIPAA Privacy Rule - What You Need to Know as a Healthcare Provider
Feb 2017
Spotlight on Post Market Surveillance
Feb 2017
How to Determine Which Jurisdiction`s Employment Laws Reach Border-Crossing Staff
Feb 2017
The NAFTA (Canada, Mexico, US) Rules of Origin and Certificate of Origin Requirements
Feb 2017
Techniques to engage information workers to improve Information Governance compliance
Feb 2017
New Fatca & Fbar Filing Requirements: Meeting the Requirements and Avoiding the Penalties
Feb 2017
How to conduct a Human Factors and Usability validation following ISO62366 and the new FDA Guidance
Feb 2017
The Basics of Professional Regulatory Law: Licensure and Certification, with an Emphasis on Health Professions
Feb 2017
CIBSE BIM Roadshow: London
Jan 2017
California Prop 65 - New Article 6 Regulations for Clear and Reasonable Warnings: What you need to Know?
Jan 2017
Risk Management for Non-Student Minors on Campus
Jan 2017
Chemistry 101 for Medical Device Regulatory & Quality Professionals: Essential knowledge needed to Manage Drug&Device Combination Product Project
Jan 2017
Countdown to Compliance Under OSHA`s Final Silica Rule: Best Practices for Developing a Written Exposure Control Plan
Jan 2017
FDA Regulation of Combination Products
Jan 2017
The Investigational Medicinal Product Dossier (IMPD): EU CTA vs. FDA IND: Comparing the Content and Agency Expectations
Jan 2017
Women`s Health, Domestic Violence and Sexual Assault Western Caribbean Cruise
Jan 2017
How to Write HIPAA Policies and Procedures
Jan 2017
FDA Food Labeling Claims - Understanding the Advantages and the Risks of Claims
Jan 2017
The Annual International Congress of the International Association of Law and Forensic Science (IALFS)
Jan 2017
Recalls, Removals, and Market Corrections in Compliance with FDA and ISO Requirements
Jan 2017
CIBSE BIM Roadshow: Birmingham
Jan 2017
Medical and Legal Issues at the End of Life
Jan 2017
Implementation of the Generic Drug Labeling Rules
Jan 2017
Judicial Imperative for Mitigating Recalls and Outbreaks in Food Industry
Jan 2017
The New FDA-Product Approval, Inspection, and Enforcement
Jan 2017
What the FDA FSMA Transportation Rules Mean for U.S. Food Importers and Foreign Suppliers
Jan 2017
Fundamentals of the de novo process for medical devices: What you need to know when pursuing a de novo application and approval with the FDA
Jan 2017
FDA Warning Letter - Consent Decree Software Validation
Jan 2017
Global Anti-Corruption & Compliance in Mining Toronto
Dec 2016
21 CFR Part 11 - Electronic Record and signature Validation
Dec 2016
Transfer of Analytical Methods and Procedures: FDA Requirements and Strategies and Tools for Implementation
Dec 2016
Awareness of Potential Food Safety Problems that Occur During Food Transportation (2)
Dec 2016
Preventing Corporate and Governmental Fraud
Dec 2016
When Regulation E and ACH Don`t Align
Dec 2016
Quality and Compliance - Building Your Key Capabilities for Future Success
Dec 2016
Clinical Evaluation Reports (CER`s) Required for All Medical Devices in Europe
Dec 2016
Application of CMS Quality Indicator Process in Healthcare Food Service
Dec 2016
FDA Action on Antiseptic Wash Products: What is Next for the Industry?
Dec 2016
Using US Customs FREE ACE Portal to Improve Import Compliance & Identify Strategic Opportunities
Dec 2016
Understanding the Mexican Standard NOM-086-SSA1-1994 for food and beverages with modifications in its composition
Dec 2016
2017 NACHA Operating Rules Preview and Update on Rules
Dec 2016
Product Risk Management Under ISO 14971:2007 and ICH Q9
Dec 2016
Clinical Trial Regulation Conference
Dec 2016
Risk Management and Compliance for Law Firms
Dec 2016
Public Sector Legal Officers’ Intensive
Dec 2016
Affordable Housing South East Asia
Dec 2016
Go Beyond ISO 9001:2015`s Requirements when Dealing with Risk
Dec 2016
Conflict Minerals Supply Chain Compliance and Transparency
Dec 2016
FDA Concepts for Medical Device Companies - Regulations, Myths, Challenges, and Best Practices – GlobalCompliancePanel
Dec 2016
Managing the IDE (Investigational Device Exemption) Submission for Compliance Success
Dec 2016
European Medical Device Regulation Workshop: Change Management
Nov 2016
Implementing a Positive Risk Culture in Government
Nov 2016
CIBSE BIM Roadshow: Manchester
Nov 2016
SA-CCR and IMM
Nov 2016
Edition Automatic Exchange of Information: The Practicalities of Reporting under CRS
Nov 2016
Challenges of Change Control: Implementation and Maintenance
Nov 2016
The Complete Payroll Law
Nov 2016
Understanding European Filing and Registration Procedures for Drug Approval
Nov 2016
Effective Complaint Handling & Medical Device Reporting
Nov 2016
Title IX and Study Abroad: Planning for Success
Nov 2016
Compliance with the European Cosmetics Products Regulation (EC) 1223-2009
Nov 2016
Negotiating and Mediating Healthcare Disputes Eastern Caribbean Cruise
Nov 2016
Negotiating and Mediating Healthcare Disputes
Nov 2016
Annual Advanced Employment Issues Symposium (AEIS)
Nov 2016
Bullet Proof 510(k) and Latest FDA Proposed Changes to the Process
Nov 2016
CGMP Quality Principles for the FDA Regulated Industries: 2-Day In-Person Seminar
Nov 2016
European Biosimilars Conference
Nov 2016
The OCR Phase 2 Audit Program
Nov 2016
The International Congress on European Regulations and Compliance for Cosmetics (CRCC2016)
Nov 2016
Overview of the Mexican Labeling Standards and the New Labeling Requirements
Nov 2016
Preparing for the Upcoming EU Medical Device Regulations
Nov 2016
Responsibilities of the HIPAA Privacy Officer - Ensuring Compliance and Avoiding Penalties
Nov 2016
Social Media Policies: Risks and Regulations
Nov 2016
Phase 2 HIPAA Audits: What to Expect and How to Pass
Nov 2016
HIPAA Security & Privacy Risk Analysis- OCR Audits
Oct 2016
How to conduct a HIPAA Security Risk Assessment and Write Policies-Brian L Tuttle
Oct 2016
Application for Investor Advisor Registration - ADV Part 1, Part 2A, Part 2B and More
Oct 2016
Mandatory GMO Labeling: Preparing for Implementation
Oct 2016
World Litigation Forum Palo Alto
Oct 2016
Remote Deposit Capture (RDC) Rules and Regulations - Legal and Compliance Requirements
Oct 2016
FDA’s New Draft Guidance on Data Integrity for CGMP Compliance
Oct 2016
Understanding the Impact of the Americans with Disabilities Act Amendments Act (ADAAA)- Steering Clear of Liability
Oct 2016
FDA Inspection: Do`s and Don`ts
Oct 2016
Adverse Event Reporting - Best Practices Dietary Supplements
Oct 2016
From Volume to Value: An Overview of MACRA, MIPS, APMs and the New CMS Quality Payment Program
Oct 2016
Federal Tax Update: Individuals (Form 1040)
Oct 2016
Substantiation of Food and Supplements Marketing Claims: FDA and FTC Requirements
Oct 2016
Tax Refund Frauds: Personal and Business Identity Theft
Oct 2016
PCI DSS Compliance in Advancement: Update for 3.2
Oct 2016
What to Do When the DOT Hazardous Materials Enforcement Inspector Comes Knocking
Oct 2016
Acceptance Activities in FDA QSR
Oct 2016
Bank Secrecy Act & Beyond: Understanding Currency and Monetary Reporting Requirements
Oct 2016
FDA Vs Health Canada
Oct 2016
Decommissioning of Nuclear Installations
Oct 2016
New DOL Regulations on Salaried Exempt Employees
Oct 2016
MATERIALS` (Ottawa, CANADA:)
Oct 2016
Supplier and Contractor Qualification and Control:
Oct 2016
Learning Design Controls through Review of FDA 483 Observations
Oct 2016
Best Practices for SOP Development and Implementation for the FDA Regulated Industry
Oct 2016
Edition of the Corporate Counsel Exchange
Oct 2016
Birth Injuries and The Law
Oct 2016
Advertising and Promotion of Dietary Supplements
Oct 2016
Preparing Managers for Layoff Communication: Practical Strategies for Notifications and Beyond
Oct 2016
Dubai Health Regulation & Medical Tourism Conference (DHRC)
Oct 2016
Chemical Safety for the Century Act
Oct 2016
Understanding Proper Labeling & Packaging Requirements & How to Stay Legally Compliant
Oct 2016
HIPAA Training for the Compliance Officer
Oct 2016
Asia-Pac Trial Master File Summit
Oct 2016
How to Conduct an Effective Annual Product Quality Review
Oct 2016
Security in Government Conference - Cancelled
Sep 2016
Pharmaceutical cGMP, Data Integrity and FDA Inspections – Current Challenges and Preparations
Sep 2016
Basel III Liquidity Rules - LCR and NSFR
Sep 2016
FDA`s Update on Elemental Impurities According to the new ICH Q3D and USP 232/233 Guidelines - Are you ready?
Sep 2016
Liquidity and Funding Risk USA
Sep 2016
GCP: The IND, How to Gain Approval for Clinical Trials in the USA
Sep 2016
FDA Regulations for Marketing Dietary Supplements in the U.S
Sep 2016
Child and Spousal Support (Part I)
Sep 2016
Implementing and Monitoring AML/CTF Programs: 2-Day Workshop
Sep 2016
What to Expect in a Federal HIPAA Audit & How to Avoid a Federal Audit
Sep 2016
Port Finance International Casablanca
Sep 2016
Annual Pharmacovigilance Asia
Sep 2016
FDR Oversight Best Practices Summit
Sep 2016
Regulatory Document – Site Master File
Sep 2016
Quality Metrics Program: FDA Challenges and Requirements including the New `Quality Metrics Technical Conformation Guide` Released
Sep 2016
Global Focus: A Guide to Identifying PEPs and Meeting Anti-Bribery and Corruption Obligations
Sep 2016
The Mastering the CMS Program Audits Summit
Sep 2016
Annual XVA Forum: Funding, Capital and Valuation
Sep 2016
Implementing ISO 13485:
Sep 2016
Good Documentation Practice for GxP Environments
Sep 2016
Medical Record Standards: What Hospitals Should Know About the CMS Hospital CoPs
Sep 2016
Understanding Pay Equity, Discrimination and Reporting Requirements
Sep 2016
21 CFR Part 11/Annex 11 compliance for software validation and SaaS
Sep 2016
How to avoid misclassification: Independent Contractor (Self-Employed) or Employee?
Sep 2016
FDA`s Pet Food Labeling Guidelines
Sep 2016
Medical Ethics and Legal Medicine
Sep 2016
Estate Planning for and Beyond
Sep 2016
Annual Managing Insurance Assets
Sep 2016
IRS Enforcing Due Diligence Rules against Return Preparers
Sep 2016
FDA and CFIA-Overview of Proposed Regulations - Let`s Get Updated
Sep 2016
Defining and Managing Protocol Deviation/Violation/Exception
Sep 2016
Get ready for your HIPAA Compliance Audit
Sep 2016
Registering Your Brand Name and Logo with the USPTO
Sep 2016
ASQ Certified Quality Engineer (CQE) Exam Preparatory Course - Webinar Series
Sep 2016
IACSP ASEAN Security Awards & Symposium
Sep 2016
Title IX and Protecting the Rights of the LGBTQ+ Community on Your Campus
Sep 2016
Medical Device Tracking: Latest FDA Update and Expectations
Sep 2016
Subordinated Debt Financing from Non-Profit Lenders
Sep 2016
SGEM International Scientific Conference on Economics, Finance and Law
Aug 2016
FDA Regulation of Digital Health - Current Status and Recent Developments
Aug 2016
Business Continuity or Disaster Recovery Planning
Aug 2016
Project Financial Modelling
Aug 2016
Logistics Channel Incoterms Standards
Aug 2016
Building a Vendor Qualification Program for FDA Regulated Industries
Aug 2016
Cuba Sanctions: All You Need To Know
Aug 2016
Internship Programs: Limiting Potential Liabilities
Aug 2016
Mastering Risk Based Internal Auditing (RBIA)
Aug 2016
Lyophilization: What you Need to Know, Validation and Regulatory Approaches
Aug 2016
Changes to the Common Rule (45 CFR 46) : What this means for you
Aug 2016
FDA Compliance and Clinical Trial Computer System Validation
Aug 2016
Challenges of the and Week Payrolls and How to Overcome Them
Aug 2016
Employee Leave Abuse (FMLA & ADA/ADAAA)
Aug 2016
How to do a Risk Analysis
Aug 2016
Regulatory Update: FINCEN`s New CDD Rule and the New Prong of the AML Program
Aug 2016
Customs-Trade Partnership Against Terrorism (C-TPAT) and Supply Chain Security
Aug 2016
FSMA Gives FDA Recall Authority Over Adulterated Food and Broadens Standards for Food Detention
Aug 2016
Health Care Reform - New and Current Issues Regarding the Affordable Care Act (Obamacare)- Part 2
Aug 2016
Medical Ethics and Legal Medicine
Aug 2016
Data Integrity: FDA, WHO and EMA`s Requirements
Aug 2016
FDA Scrutiny of Purchasing/Supplier Controls
Aug 2016
How to Prepare for Increased HIPAA Enforcement
Aug 2016
Interpreting and Reporting Descriptive Statistics
Aug 2016
Mastering Negotiation Skills: Win-Win Tools to Advance Your Business Objectives
Aug 2016
Are You Ready For The FDA`s Mandate Requiring Electronic Submission Conformance to SEND and SDTM?
Aug 2016
Process Validation Guidance Requirements (FDA and EU Annex 15: Qualification and Validation)
Jul 2016
Considerations for a Successful Biosimilars Program
Jul 2016
Bullying Versus Harassment: Understanding the Difference and Protecting Yourself from Both
Jul 2016
Risk Assessment and Business Impact Analysis using PMI and ISO/IEC 21500 Project Management Methodologies
Jul 2016
Health Canada`s Regulations on Natural Health Products vs. FDA`s Dietary Supplement Regulations
Jul 2016
340B Compliance and Self audits
Jul 2016
Why is FDA at my facility, and what do I do during an inspection?
Jul 2016
How to Conduct a Human Factor Analysis of Instructional Documents, Particularly Master Batch Records (MBR) and Standard Operating Procedures (SOP)
Jul 2016
Tools and Techniques for Operational Risk Management: Regulatory Aspects
Jul 2016
Navigating through Maze of In-vitro Diagnostics (IVD) Regulations: A systematic approach from Regulatory Strategy to Regulatory Approvals in U.S./Europe/Canada
Jul 2016
FDA`s Emerging Signals Guidance: Reporting Medical Device Safety Warnings
Jul 2016
Designing a Supplier Qualification Program
Jul 2016
You Said Whaaat? Limiting Employer Liability for Sexual Harassment in the California Workplace
Jul 2016
SharePoint Governance for the End User Community
Jul 2016
Proper CAPA Management and Root Cause Analysis
Jul 2016
Title 19 Customs Duties Parts 200 to End, Revised
Jul 2016
Process Validation - Current Industry Practices and FDA Guidance Document Review
Jul 2016
Overview of the Foreign Corrupt Practices Act
Jul 2016
Overview of FDA Regulation of the Tobacco Industry
Jul 2016
USP <71> Sterility Testing: New Harmonization with International Compendia and Overview
Jul 2016
Radar Imaging For Next-Generation Security Systems Masterclass
Jul 2016
SUDEP `16 / International Sustainable Development on Economy and Planning Conference
Jul 2016
IBMC `16 / International Business Management Conference
Jul 2016
Risk OTC Derivatives Clearing Summit
Jun 2016
Set-Up of Insurer Bad Faith, Defense of Bad Faith Suits
Jun 2016
Writing Effective Environmental Impact Statements (EIS) Under National Environmental Policy Act (NEPA)
Jun 2016
OSHA Recordkeeping: What to Save, What to Delete, and Everything In-Between
Jun 2016
Process for Performing a Vendor/Contract Audit: What Should be Considered and How to Plan, Perform and Report Results of a Vendor Audit
Jun 2016
Lending Compliance Update
Jun 2016
Initial Margin and Funding
Jun 2016
Blockchain and Distributed Ledgers in Financial Institutions
Jun 2016
Texting and E-mail with Patients: Patient Requests and Complying with HIPAA
Jun 2016
IRS Update
Jun 2016
Annual Capital Modeling in Insurance
Jun 2016
Globalization of Competition Policy
Jun 2016
Comparison of GFSI with FSMA requirements
Jun 2016
Universal Design: Proactively Addressing Accessibility on Campus
Jun 2016
Food Contact Training
Jun 2016
Understanding and Implementing the EU Vigilance System
Jun 2016
Clinical Quality & Compliance Masterclass
Jun 2016
Understanding and Implementing the Medical Device Directive: 2-Day In-person Seminar
Jun 2016
Pharma IT Compliance
Jun 2016
Pharmapack North America
Jun 2016
Loan Portfolio Management and Review - Regulations, Process, Loan Grading Techniques, Collateral and Documentation
Jun 2016
Background Checks in California: Best Practices for Hiring in the Golden State
Jun 2016
Alternative Withholding Methods: Income Tax Computations for Special Situations
Jun 2016
The Past Isn`t in the Past`: Effecting Sound Employment Background Checks in California
Jun 2016
FDA`s Low-Risk Device Policy and the Impact on Mobile Medical Device Applications
Jun 2016
Gluten-Free Labelling with a Special Focus on Fermented, Hydrolyzed or Distilled Foods: How to Prove & Display It Correctly
Jun 2016
Vision 2030 Summit
Jun 2016
Pharma, Pricing & Marketing Access
Jun 2016
Compliance with U.S. Securities and Exchange Commission Laws
Jun 2016
Electronic Data Integrity in a GxP Environment: Managing the Data Lifecycle for Compliance
Jun 2016
International Academic Conference on Education and Social Sciences (IACESS)
Jun 2016
IIPLA Global IP Summit London
Jun 2016
Doctors in the dock - gross negligence manslaughter and medical expert witness
Jun 2016
Mexico Maquiladora/IMMEX and their Free Trade Agreements
Jun 2016
IDMP Implementation & Data Management
Jun 2016
Performing Anti-Fraud Audits in Purchasing and Accounts Payable
May 2016
Copyright for Online Course Materials
May 2016
Legally Compliant Employer-Employee Arrangements: Non-Compete Agreements, Classifying Independent Contractors vs. Employees, and Employment-Related Contracts
May 2016
GMPs for OTC and Cosmetic Products - US and Global Requirements
May 2016
Implementing Advanced Pivot Table Techniques
May 2016
CMS Proposed Changes to the Discharge Planning Standards and the IMPACT Act
May 2016
Annual Project Finance In Renewable Energy
May 2016
Payroll Recordkeeping Compliance
May 2016
International Technology Law Association (ITechLaw) World Technology Law Conference
May 2016
Bitcoin Conference Prague
May 2016
Improving performance against the NSQHS standards
May 2016
Key Factors to Develop HIPAA Policies and Procedures
May 2016
Medicare Penalties and Incentives- Updates for Medical Practices
May 2016
Building a Sustainable Validation Program from Top to Bottom
May 2016
Lifecycle Approach to Analytical Methods: Incorporating QbD Principles into Method Development, Validation and Transfe
May 2016
Advertising and Promotional Material Compliance and Review Process
May 2016
Final FSMA Subpart G Rule Requirements for the Receiver Liability for Supplier Preventive Controls
May 2016
Advanced Consumer Lending - Process, Best Practices, 6Cs of Credit, Loan Structuring and Pricing
May 2016
Importing Marketing Channel Audits
May 2016
Legal Hiring and Termination
May 2016
Final revised Draft to ISO 14644 Parts 1 and 2 changes Classification and Monitoring Methods: Are you prepared?
May 2016
Understanding Disclosures, Certifications and Corporate Responsibility Relating to SOX - Sections 302, 401, 404, 409, 906
May 2016
GMP Complaint Systems and Product Recalls
May 2016
WACOSS
May 2016
Italian ePharma Day
May 2016
Implementing Validation and Qualification - Annex 15 and FDA Requirements
May 2016
I`m Out`a Here! Successfully Navigating the California Family Rights Act (Part – I)
May 2016
Evolution of Board Responsibility for Compliance Program Oversight
Apr 2016
USP [800] - Guidelines for Safe Handling of Pharmaceuticals
Apr 2016
The Trans-Pacific Partnership: Opportunities & Risks
Apr 2016
Cosmetics Compliance Summit
Apr 2016
Best Practices for Compliance with FDA 21CFR1040
Apr 2016
Personal Moscow Exhibition for HRM, Training and Development
Apr 2016
Nordic ePharma Day
Apr 2016
3 Ways to Avoid Costly Wage and Hour Problems
Apr 2016
The Regulatory Framework in Europe
Apr 2016
Edition Automatic Exchange of Information: CRS and FATCA
Apr 2016
XVA Model Validation and Development
Apr 2016
FDA NLEA Regulation for Retail and Foodservice Labeling - An Overview of Current Regulation and Pending Regulations
Apr 2016
Do`s and Don`ts of Effective HIPAA Compliance program for BYOD & Mobile Devices: Be Prepared for what`s new in !
Apr 2016
Non-Resident Employee Tax Withholding
Apr 2016
Staying in Compliance with the Federal Debt Collection Practices Act (FDCPA): What Debt Collectors can Say or DO?
Apr 2016
Elemental Impurities: The New Requirements
Apr 2016
Packaging and Labeling for Commercial and Clinical Products
Apr 2016
International Conference on Globalization Enterprises and Economic Development
Apr 2016
Identifying and embedding learning from claims and inquests
Apr 2016
FDA New Electronic Data Capture Guidance - What is the impact on Inspectional Record Requirements
Apr 2016
Preparing to Comply with the New FDA FSMA Rules
Apr 2016
Annual Constitutional Cases Conference
Apr 2016
Complying with the GDPR: International Data Protection and Privacy Excellence Forum
Apr 2016
The New Clinical Trial Regulation
Apr 2016
How Fixing FDA Compliance Problems (Remediation) Aligns with the 5 Stages of Grief
Apr 2016
How the FDA & FTC Regulate Advertising & Promotion of Drugs & Dietary Supplements
Apr 2016
Employee Settlement Agreements in : Make Sure You Get Them Right - FLSA, EEOC, ADEA & NLRB
Mar 2016
Russia and CIS Summit on Anti-Corruption
Mar 2016
Evaluating the Effectiveness of a Corporate Compliance Program
Mar 2016
The Federal False Claims Act and the Anti-Kickback Statute: Is Your Organization at Risk
Mar 2016
Introduction to Country of Origin: Essential Practices for Import Management
Mar 2016
FMLA, ADA, USERRA, Workers Compensation, and HIPAA : Navigating the Bermuda Triangle of Medical Leaves
Mar 2016
Liquidity Management, ALM and FTP
Mar 2016
Optimizing Target Weights for Foods and Beverages
Mar 2016
Ensuring Compliance of Your Bioanalytical Method Validation with the 2013 FDA Draft Guidance
Mar 2016
Office of Inspector General (OIG) Work Plan : Trends, Reports and Issues
Mar 2016
Obligations, Responsibilities and Warranties of the RDFI and ODFI for Special Processes: Returns & NOCs - the RDFI processes-Part 1
Mar 2016
Top 10 ACA Traps for the Unwary - What you should know about The Affordable Care Act (ACA) before the Reporting Deadline
Mar 2016
AML Investigations and SAR Preparation
Mar 2016
How to Apply ISO 27001 Principles to Enterprise Risk Management in
Mar 2016
Agribusiness in Ukraine
Mar 2016
Conference on Asian & Middle Eastern S​tudies
Mar 2016
DOL`s New Proposed Overtime Pay Regulations & Proposed Rules - What to Expect and How to Comply
Mar 2016
Auditing Hospital-Physician Arrangements & Contracts under the New Stark Rules
Mar 2016
HR and the Law : Ensure Policy Meets Practice
Mar 2016
Antimicrobial effectiveness test USP [51] : Overview and New Content Proposals
Mar 2016
Trade Measures and WTO
Mar 2016
Annual Regulatory Reporting
Mar 2016
The importance of Detecting Truth, Deception, and Lies while conducting an Investigative Interview
Mar 2016
Regulations & Operational Compliance for Funds
Mar 2016
Confined Space Entry Regulation Requirements
Mar 2016
Device Changes and the 510(k)
Mar 2016
Understanding Incident-To Compliance
Mar 2016
Clinical Research for Cardiovascular Pharmaceuticals: Ensuring Compliance of Traditional and New Cardiovascular Medications
Mar 2016
Fraud and Abuse in the Sales & Marketing of Medical Devices
Mar 2016
Training Your Title IX Hearing Boards
Mar 2016
CIS Pharmaceutical Forum
Mar 2016
Developing a Title IX Mandatory Reporting Training Program
Mar 2016
ERISA Litigation
Mar 2016
Integer Emissions Summit Brazil
Mar 2016
Annual Advanced ITAR Compliance and Export Controls EAST COAST
Feb 2016
Building an effective AML Program and Best Practices for Sanctions Screening
Feb 2016
Guidelines for Performing Fraud Risk Assessment and How to Conduct an Internal Fraud Investigation
Feb 2016
How to Avoid and OCR HIPAA Audit
Feb 2016
Root Cause Analysis - The Heart of a Successful CAPA Program
Feb 2016
Edition Stress Testing
Feb 2016
Regulatory Affairs aspects of clinical trials and clinical Product Development in the EU
Feb 2016
The CMS Restraint and Seclusion: Navigating the Most Problematic of all of the CMS Standards
Feb 2016
Annual Holistic Approaches to Collateral Management in the New Regulatory Environment
Feb 2016
Booming Service Sector: From Achievements to Growth Prospects”
Feb 2016
Sterilization Processes: The Methods, Parameters and Deficiencies Often Cited
Feb 2016
Creating Effective SOP for Regulatory Compliance
Jan 2016
Stress-Testing for Financial Institutions, Beyond Regulatory Constraints
Jan 2016
Annual Financial Crime Asia Summit
Jan 2016
Exporting to Mexico Webinar Series 3: INCOTERMS Review and INCOTERM Common Practices in Mexico
Jan 2016
SkyTech Drone Expo
Jan 2016
Voyage Accident, Engineering Damages Investigation & Dispute Resolution
Jan 2016
Managing Student Activism
Jan 2016
International Compliance and Legal Risks Conference
Jan 2016
Payroll Technology
Jan 2016
Controlling Human Error in the Manufacturing Floor
Jan 2016
How to Develop a strong CAPA System by Understanding its Unique Challenges
Jan 2016
Winter Investment Forum
Jan 2016
All You Need to Know About Same Day ACH - Faster Payments!
Jan 2016
Social Media as a Recruiting Tool: Strategies for Using Facebook, Twitter, and LinkedIn
Jan 2016
Good Social Media Practices to Avoid FDA Actions
Jan 2016
FSMA Final Rules for Preventive Controls for Human and Animal Food
Jan 2016
Effective Design Controls in Accordance with Subpart C of 21 CFR, Part 820
Jan 2016
Preparation is the Best Medicine: Getting Ready for OSHA`s New Strict, Expanded Enforcement against the Healthcare Industry
Jan 2016
Cleanroom Monitoring & Maintaining a Quality Environment : Overcoming USP [797] Common Non-Compliance Issues
Jan 2016
Trends in U.S. Payments Landscape - Tokenization, EMV/NFC and How it Affects Merchants Accepting Payments
Jan 2016
Intro to Government Contract Proposals
Jan 2016
The HIPAA HOT List: Key Issues in HIPAA Compliance Today
Jan 2016
Established Condition - The New FDA Guidance
Jan 2016
Drug Master Files: New Implications under GDUFA
Jan 2016
U.S. FDA`s Strategic Priorities - and Beyond
Jan 2016
Design Inputs - Design Outputs Traceability Matrix - Principles of Lean Documents and Lean Configuration
Jan 2016
Exporting to Mexico Webinar Series 2: How to Settle Disputes with Mexican Customs
Jan 2016
Implementing the ACA, HIPPA, and Discrimination Laws into Your Organization`s Wellness Strategy
Jan 2016
AML/OFAC Risk Assessment: The Cornerstone of an Effective Compliance Shop
Jan 2016
Statistical Process Control
Jan 2016
FDA Inspections : Managing the Myth and the Reality
Jan 2016
Avoiding 12 Most Common Statistical Errors in Clinical Research
Jan 2016
Last Minute Update: Hidden Changes to 2015 and Income Tax and Information Reporting Forms
Jan 2016
Usability Engineering in IEC 62366-1:2015 - Implementing the New Standard
Jan 2016
Investigating sudden unexpected death
Jan 2016
Risk Management and Risk-Based Monitoring
Jan 2016
Creating and Maintaining a GMP Quality System
Jan 2016
How to Detect Lack of Data Integrity
Jan 2016
How to Identify, Investigate, Deny and Terminate FMLA Abuse
Jan 2016
Process Robustness: The New FDA Paradigm
Jan 2016
Environmental Monitoring: Prepare Your Company to Meet Final FSMA Rule Requirements
Jan 2016
FDA`s New Enforcement of 21 CFR Part 11
Jan 2016
Incorporating Risk Management into Process Improvement
Jan 2016
FDA Compliance and GAMP V Computer System Classification
Jan 2016
Establishing a Service Level Agreement (SLA) Process
Jan 2016
Writing Effective Standard Operating Procedure (SOPs)
Jan 2016
Safer Consumer Products Briefing
Jan 2016
How to Respond to an FDA Investigation: What happens when the FDA threatens to shut you?
Jan 2016
Aviation Security Summit (AVSEC)
Dec 2015
Basics of US Medical Device Regulation
Dec 2015
Complaint Handling Requirements - Interrelationship with CAPA, Change Control, Adverse Event Reporting and Recalls, Life Cycle Process Activities
Dec 2015
New HIPAA Audit and Enforcement Activities: Being Prepared to Show your Compliance
Dec 2015
Validation and Part 11 Compliance of Computer Systems and Data Australia
Dec 2015
Paediatric Drug Development - Adult Data and Relevant FDA Laws
Dec 2015
European Payments Regulation
Dec 2015
HIX Compliance Summit: and HIX Risk Adjustment
Dec 2015
Food Law - Master of Laws (LLM) by Distance Learning (run by De Montfort University)
Dec 2015
French ePharma Day
Nov 2015
Cloud Law European Summit
Nov 2015
Smarter Borders
Nov 2015
Sales Tax - Avoiding Double Taxation on Drop Shipments
Nov 2015
HIPAA Compliant Patient Engagement: New Rules on Email and Text (SMS) for Health Care Providers and Business Associates
Nov 2015
Margin Requirements for Non-Centrally Cleared Derivatives
Nov 2015
Effective Quality Audits: Digging Deep
Nov 2015
Ensure Compliance to FDA`s Design Control Requirements using Requirements Management Techniques
Nov 2015
US Regulatory Affairs: A Comprehensive Review
Nov 2015
Computer System Validation for Systems Supporting Clinical Trials
Nov 2015
Legal & Regulatory Compliance Executive Boardroom
Nov 2015
Reducing your Exposure to a GMP FDA Warning Letter
Nov 2015
Corrections and Removals - Understanding and Implementing the Final Guidance Document
Nov 2015
Audit program (Internal & External) for Clinical trial sites
Nov 2015
Banking and Marijuana: When Federal and State Laws Collide
Nov 2015
AML High-Risk Transactions - Identifying and Managing Them
Nov 2015
ICH-FDA Good Clinical Practice – Managing Clinical Trials
Nov 2015
Current Legal and Regulatory Challenges for HR
Nov 2015
Best Practices For Preparing For an ISO Audit
Nov 2015
Acute behavioural disorder - the myths and the reality
Nov 2015
Confined Space Rules for Construction that are in the Final OSHA Rule
Nov 2015
Title IX: 5 Things Every Department Chair Needs to Know
Nov 2015
Building a Vendor Qualification Program for FDA Regulated Industries
Nov 2015
FDA New Electronic Data Capture Guidance- Inspectional Record
Nov 2015
Business Plans That Get Results
Oct 2015
An Easy to Implement Integrated Risk Management Approach Compliant with ISO 14971
Oct 2015
Risk Based Approach to Software Quality Validation
Oct 2015
Essentials of Lobbying
Oct 2015
Clinical Trials Workshop
Oct 2015
European Automated Truck Conference
Oct 2015
Commercial & Government Microgrids Summit
Oct 2015
Technology/Analytical Method Transfer
Oct 2015
Environmental Law & Regulation for Oil & Gas
Oct 2015
EPA Clean Power Plan Implementation Summit
Oct 2015
Drug Product-Injury Litigation: Effective Use of Medical Information and the Scientific Literature in Building a Strategy for Defense
Oct 2015
Computer System Validation - Reduce Costs and Avoid 483
Oct 2015
UK ePharma Day
Oct 2015
How to manage a successful health authority interaction
Oct 2015
A look at 510(k) changes
Oct 2015
Ethics for Litigation Attorneys
Oct 2015
Humanitarian Congress Berlin
Oct 2015
Computer System Validation - Reduce Costs and Avoid 483
Oct 2015
Annual Oil and Gas International Licensing Summit
Oct 2015
Impact on Exporters of Foreign Assets Control, Anti-Boycott and Anti-Money Laundering Regulations
Oct 2015
Global Investigations Summit
Oct 2015
Creation of DHFs, DMRs, and DHRs utilizing the principles of Lean Documents and Lean Configuration
Oct 2015
Supply Chain Profitability - Achieve Competivitive Edge by Reducing Costs & Improving Performance
Oct 2015
Complying with SSA and IRS Rules for Correcting Forms W-2 and 941
Oct 2015
Changes under the HIPAA Omnibus Rule - What`s New
Oct 2015
Regulatory Aspects of Advanced Therapy Medicinal Products in the EU
Oct 2015
Risk Management in Clinical Trials
Oct 2015
Establishing an FDA-Compliant UDI System
Oct 2015
ABHI Regulatory Conference
Sep 2015
China Smart Grid Forum
Sep 2015
Solvency II: ORSA and Pillar 3 Reporting
Sep 2015
Mini-LLB for Regulators
Sep 2015
Evidence-Based Policy Making
Sep 2015
Conducting Regulatory Investigations
Sep 2015
Operational Risk for Financial Institutions - Beyond Regulatory Constraints - By Compliance Global Inc.
Sep 2015
Practical Approaches to Implementing OECD Common Reporting Standards
Sep 2015
The Logistics and Law of Exporting from the United States
Sep 2015
PT / EXPO COMM CHINA
Sep 2015
Marketing Products without Getting Hammered by FDA
Sep 2015
Seven Step Compensation Diet
Sep 2015
Annual Balkans, Black Sea and the Adriatic Oil and Gas Summit
Sep 2015
FDA Inspections: Preparation and Managing the Consequences
Sep 2015
Calibration and Qualification in Analytical Laboratories
Sep 2015
How can Vendor- Sponsor Collaborate to Deliver a Quality Service
Sep 2015
California Laws- Pregnancy Disability Leave- Ban the Box
Sep 2015
US Drug Supply Chain Security Act - Serialization & Validation for Track & Trace Compliance
Sep 2015
Australian Competition Policy
Sep 2015
Creating Design History Files (DHF), the Device Master Records (DMR) and the Device History Records (DHR), Utilizing the Principles of Lean Documents and Lean Configuration
Sep 2015
Tackling Methamphetamine
Sep 2015
Marketing Products without Getting Hammered by FDA
Sep 2015
Health Care Reform and Review of Affordable Care Act Requirements
Sep 2015
The New Medical Device Regulation Information Day
Sep 2015
Tax Planning for the Wealthy Family
Sep 2015
FDA 510(k) Requirements, Submission, and Clearance: Best Practices
Sep 2015
Application of Lean Six Sigma Methodology for Regulated Industries
Sep 2015
Regulatory Expectations-Best Practices in Asset Liability Management
Sep 2015
When is Overtime Pay Required- FLSA Regulation
Sep 2015
Highest Risk Factors with HIPAA
Sep 2015
Consensus
Sep 2015
Understanding the Implications of FDA 483s and Actions to Avoid Further Regulatory Actions
Sep 2015
Kalimantan Coal Conference
Sep 2015
The Anti-Kickback Statute: Paying for Referrals is a Bad Idea
Sep 2015
CLOs - Analysis of Lenders
Sep 2015
Bullet Proof 510(k) - Latest FDA Proposed Changes to the Process
Sep 2015
Aboriginal Consultation & Collaboration for Energy
Aug 2015
Corrective Actions - Current Expectation of ISO 13485 and FDA Auditors
Aug 2015
Sanitary Food Packaging Concepts-Food Safety Training
Aug 2015
Regulatory Inspection at Your Food Facility- Food Safety Guidelines
Aug 2015
ISO/FDIS 9001: - Planning for the Changes
Aug 2015
Increasing Margin through Trade Compliance-How To Cut Cost
Aug 2015
Banking Regulations -, Federal Banking Regulations
Aug 2015
The Federal False Claims Act: Enforcement and the Obamacare Expansion
Aug 2015
Annual Land Access Forum
Aug 2015
Orphan Drugs: the Conundrum- Clinical Research Trials
Aug 2015
Training in Regulated Environments- Regulatory Compliance Training
Aug 2015
Creating a Global Regulatory Plan
Aug 2015
Understanding ISO 13485-FDA Requirements for Medical Devices
Aug 2015
System Development Life Cycle (SDLC) Methodology and FDA-Regulated Systems
Aug 2015
Preparing for Imminent Federal Hipaa Audits (level:intermediate)
Aug 2015
Legal and Effective Behavioral Interviewing
Aug 2015
Understanding FDA Regulations and Role in Opioid Pain Management
Aug 2015
Failure Mode and Effects Analysis for Design Improvement and Design Control
Aug 2015
Understanding the Mobile Medical Applications Guidance
Aug 2015
API 570 Piping Inspector Certification Preparatory Course
Jul 2015
Export to Mexico Documentation & Procedures
Jul 2015
How To Avoid FDA 483’s/ Warning Letters? What to Do If You Happen to Get One?
Jul 2015
Paediatric Drug Development - Adult Data and Relevant FDA Laws
Jul 2015
B2B Payments -Compliance Issues Faced in
Jul 2015
Food Regulations and Labelling Standards Conference
Jul 2015
FDA Inspection and Medical Device Design Control
Jul 2015
Tips for creating Social Media strategy and policy
Jul 2015
E-Compliance: Know Your Internet rights- Cyber Security Laws
Jul 2015
FERPA Essentials for Faculty
Jul 2015
Expanded Access Programs
Jul 2015
Validation of Complex Cell-Based Potency Methods
Jul 2015
Conducting Effective FMEA to address JCAHO Requirements
Jul 2015
Navigating the New FDA Draft Guidance on ISO 10993: Biological Evaluation of Medical Devices
Jul 2015
Canadian Site Licence Applications for Dietary Supplements. - By Compliance Global Inc
Jul 2015
Canadian Product Licenses for Dietary Supplements. - By Compliance Global Inc
Jul 2015
HIPAA Fundraising Strategies: Compliant, Proper use of Protected health Information. - By Compliance Global Inc
Jul 2015
Technical and Regulatory Writing for FDA Regulated Industries
Jul 2015
Pharmaceutical Registration Strategies in Europe & the US for Generics & Super Generics
Jul 2015
Computer System Validation to Mobile Applications-Live Training
Jul 2015
CDOI: Compliance with the California SIU Regulations
Jul 2015
Canadian Establishment Licenses: Drugs, Supplements and Medical Devices
Jul 2015
Using Q-Submission to Most Effectively Prepare for an FDA 510(k) Submission
Jul 2015
Solar Finance & Investment Asia
Jun 2015
Simple Substantial Economic Effect Regulatory Compliance
Jun 2015
McNamara-O’Hara Service Contract Act-Online Training
Jun 2015
Power Plant Decommissioning Retirement & Remediation
Jun 2015
Normality Tests and Normality Transformations
Jun 2015
Optimising Regulatory Reporting for Banks
Jun 2015
European Regulation Roadshow - Copenhagen
Jun 2015
IDMP Compliance Challenge and Regulatory Information Management
Jun 2015
Submitting Marketing Applications in Canada
Jun 2015
Build a Compliance Program for Healthcare Providers, Health Insurance Companies and Business Associates
Jun 2015
Treasury Management - Liquidity, Interest Rate, Foreign Exchange and Capital Risk Management
Jun 2015
Insurance Risk EMEA
Jun 2015
Bloodborne Pathogen
Jun 2015
International Product Registration: What documents are required?
Jun 2015
Manage Your FDA Inspection Before It Happens
Jun 2015
U.S. FDA`s New Strategic Priorities 2014 - 1018 ()
Jun 2015
Writing Evaluation Reports-How to Write Evaluation Report
Jun 2015
Project Scheduling, Risk Analysis and Cost Control
Jun 2015
AFR National Infrastructure Summit
Jun 2015
Green Evolution : Global Construction Materials and Technologies
Jun 2015
Ending Domestic Violence
Jun 2015
A+ Compliance with Pregnant Employees and New Parents: Pregnancy at Work
Jun 2015
Civil Monetary Penalties-Civil Monetary Penalties Law
Jun 2015
The Ultimate Guide to Navigating California Medical Leaves: The Ultimate Guide to PDL, FMLA, FEHA, SDI, CFRA, PFL, ADA and Workers Compensation
Jun 2015
Developing the Master V&V Plan to Meet U.S. FDA, ISO 13485 and 14971 Requirements
Jun 2015
Capital Management & Risk
Jun 2015
Annual Clinical Research in Turkey Middle East & North Africa Leaders Forum
Jun 2015
Conducting Observational Studies in US, Canada and Europe
Jun 2015
How to Most Effectively Prepare for and Manage FDA Inspection: Best Practices
Jun 2015
EVCA CFO Forum
Jun 2015
European Regulation Roadshow - Paris
May 2015
Monitoring Plans: 10 Rules of Effective Writing of Monitoring Plans
May 2015
Administrative Law in Professional Licensing Actions
May 2015
The safety of vulnerable patients: 8 years under the Mental Capacity Act
May 2015
The Complete 1099, 1042-S and FATCA Compliance Update
May 2015
The FDA Inspection: Preparation, Management, and Follow-Up
May 2015
The Canadian Food Label
May 2015
An Introduction to Medical Device Software: Regulations & Requirements
May 2015
Class Actions West
May 2015
California Laws Regulating Employment Screening and Safe Hiring
May 2015
Global Anti-Corruption & Compliance in Mining London
May 2015
CAPA, Failure Investigation and Root Cause Analysis - FDA Expectations
May 2015
IFRS Basics with US GAAP Comparison
May 2015
Ensuring Data Integrity for FDA/EU Compliance
May 2015
Understanding the New Custom Device Exemption Guidance
May 2015
Managing FDA After a Bad Inspection
May 2015
Complying with Section 702 of the Choice Act
May 2015
Digital ID World Middle East
May 2015
Importing and Exporting Medical Devices: A Primer on Regulatory Strategy and Requirements
May 2015
Part 2 - Quality Management System effectiveness: ICH Q10 principles, impact of failure on COGS, principles of QRM, what you can impact in reactive versus proactive
May 2015
Implementing an FDA-Compliant Medical Device Design Control Including DHF, DHR, and DMR
May 2015
Regulatory Aspects of Advanced Therapy Medicinal Products in the EU
May 2015
FDA Inspections: Before, During and After
May 2015
Your Social Media Marketing is Under FDA`s Microscope
May 2015
What To Do If the Government Comes Knocking
May 2015
Homeland Security Congress
Apr 2015
Health Canada`s Enforcement of the Regulatory Requirements for the Manufacture, Advertising and Sale of Foods and Beverages
Apr 2015
Foreign Corrupt Practices Act (FCPA) and International Anti-Bribery Course [Course-1]
Apr 2015
Oil & Gas Africa
Apr 2015
Proactive Approaches to Regulation in Transaction Banking
Apr 2015
Occupy Movements, Free Speech Zones, Social Media, and More: Managing Student Activism on Your Campus
Apr 2015
WealthPro Russia St. Petersburg
Apr 2015
Mergermarket Technology Forum
Apr 2015
Global and FDA Regulation of Electronic Cigarettes
Apr 2015
Annual Benchmarking Market Integrity and Transparency in Energy Trading
Apr 2015
WealthPro Russia Moscow
Apr 2015
Regulatory Affairs und - Compliance Pharma
Apr 2015
Regulatory Compliance for Dietary Supplements in the US, EU and Canada
Apr 2015
UDI Implementation
Apr 2015
Canadian Immigration Summit: Towards a National Immigration Action Plan
Apr 2015
Regulatory Developments in ABS Markets
Apr 2015
Fundamentals of Administrative Law
Apr 2015
Countering Online Extremism
Apr 2015
Quality System Regulations for Devicemakers: A Regulatory Approach
Apr 2015
Annual International Symposium on Southeastern European Studies
Apr 2015
China: Compliance Processes for Life Science Products (Company Establishment, Clinical Trials, Registrations, Renewals and Supply Chain Considerations)
Apr 2015
GRUR/ AIPPI Joint Brussels Workshop `The proposed EU framework for protection of trade secrets – state of play and future challenges`
Apr 2015
Forced Degradation for Pharmaceuticals
Mar 2015
Product Standards, Menthol and FDA`s Deeming Regulation
Mar 2015
International Conference on ISO26262
Mar 2015
Biomedical Software Regulation
Mar 2015
Integer Emissions Summit India
Mar 2015
Internet of Things As An Agent for Democracy & Civic Engagement
Mar 2015
Immigration Law 101: 3 Key Issues for Compliance
Mar 2015
Dispute Resolution and Arbitration in the Oil & Gas
Mar 2015
annual Government Programs Summit
Mar 2015
Landfill Leachate International Masterclass
Mar 2015
Effective Complaint Handling, Medical Device Reporting and Recalls
Mar 2015
The Annual Police Technology Forum
Mar 2015
Prisons
Mar 2015
Manufacturing and Marketing Cosmeceutical* and Homeopathic OTCs: Complying with FDA`s Rules for Drug Products that do not require FDA Pre-Approval
Mar 2015
Wet bescherming Persoonsgegevens Cursus
Mar 2015
Introduction to the Crop Protection Industry in the EU
Mar 2015
Preventing Faculty Discrimination with Case Law and Statistics
Mar 2015
How to Successfully Manage an FDA High Risk Inspection
Mar 2015
Optimising Operational Processes in the Energy Trading Market
Mar 2015
International Conference on Private Law (ICPL)
Mar 2015
Better Alternatives to Sampling Plans
Mar 2015
Bi-Annual Compliance Conference
Mar 2015
Application of Disinfectants and Sterilants to Control Microorganisms; FDA Endotoxin Test – Understanding the Latest Revision
Mar 2015
Laboratory Developed Tests under FDA`s Thumb
Mar 2015
Deconstructing Warning Letters - Using Warning Letters to Illustrate the FDA and Health Canada CFRs
Mar 2015
OSHA Inspections - Avoiding the 10 Most Common Mistakes
Mar 2015
Character of Reputation Risk: Risk or Just an Impact? Techniques for Effective Management.
Mar 2015
How to Avoid an FDA Warning Letter with a Strong CAPA Program
Mar 2015
Boards and CoSec Asia
Mar 2015
Labor and Employment Law Update
Mar 2015
Edition in Data Protection Series: Data Protection and Privacy Compliance in Big Data and Cloud
Feb 2015
Payments Forum
Feb 2015
Integer Emissions Summit Russia & CIS
Feb 2015
Data Analytics Week for Government
Feb 2015
Regulatory Filing Strategies Summit
Feb 2015
The Cosmetics Regulation (EC) 1223/2009
Feb 2015
Conference in Data Series: IDMP Compliance Challenge: Progressing on Master Data and Systems Harmonisation
Feb 2015
The Impact of Dodd Frank and EMIR on Non-US Financial Institutions
Feb 2015
Ensuring Regulatory Compliance of Food Establishments
Feb 2015
Copyright and Fair Use Essentials for Faculty
Feb 2015
FDA Quality System Management for Medical Devices
Feb 2015
Corporate Governance Law 101 for Top Management to Monitor Compliance
Feb 2015
Advanced Project Management for Performance Excellence
Feb 2015
The Impact of Dodd Frank and EMIR on APAC Markets
Feb 2015
Annual Protecting & Monetising IP Assets
Feb 2015
21 CFR 11 Compliance for Excel Spreadsheet
Feb 2015
annual Unitary Patent Package Conference
Feb 2015
The FDA Medical Device Approval Process: Preparation of 510(k)s, IDEs, PMAs
Feb 2015
Title IX and Mandatory Reporting: Developing a Training Program for Your Employees
Feb 2015
The FDA 510(k) and Q-Submission: Best Practices
Feb 2015
Annual Advanced Forum on Derivatives Reform
Jan 2015
Postgraduate Diploma in Maritime Law
Jan 2015
Annual Forum on Crown Corporate Governance
Jan 2015
Annual Anti-Corruption and Compliance for the Oil, Gas and Extractive Industries
Jan 2015
Pharmacovigilance Audits and Inspections
Jan 2015
FDA proposed changes to ISO 13485: and Medical Devices Quality Management Systems
Jan 2015
Pre-Filled Syringes
Jan 2015
Biometrics for Government and Law Enforcement
Jan 2015
HIPAA Omnibus Update - Tracking Down the Details
Jan 2015
Benchmark for Cleaning Validation
Jan 2015
MiFID II: Implementation for the Energy Markets
Jan 2015
A Systematic Approach To Writing Effective Standard Operating Procedures (SOPs)
Jan 2015
Nutrition Facts - NLEA and Beyond
Jan 2015
What is the harm in that? Risk Management 101
Jan 2015
GAMP 5 as applied to FDA software validation - strategies to avoid warning letters
Jan 2015
U.S. FDA`s Strategic Priorities - and Beyond
Jan 2015
Statistical Process Control (SPC)
Jan 2015
Compliance with the European Cosmetics Products Regulation (EC) 1223/2009
Jan 2015
Clery Act Checklist: 10 Steps for Compliance
Jan 2015
IP Leadership Forum
Jan 2015
International Intellectual Property Law Association Annual Congress (IIPLA)
Jan 2015
QUANTITATIVE EVALUATION AND MANAGEMENT of Cross Contamination Risks in Multi-Product Facilities
Jan 2015
Lex-Informatica : Cyber law, ICT Law, Information Ethics Conference
Dec 2014
FDA Decisions For IDE Clinical Investigations
Dec 2014
Regulatory Updates in China: APIs & Dossier Submissions
Dec 2014
cGMPs Beyond 21 CFR 110
Dec 2014
Developing an Efficient Relationship with FDA
Dec 2014
International Conference on Economic, Accounting, Management and Social Science
Dec 2014
FT Frontier Markets Summit
Dec 2014
The Drug Approval Process: Preparation and Processing of INDs and NDAs
Dec 2014
National Domestic Violence Conference
Dec 2014
The Drug Approval Process: Preparation and Processing of INDs and NDAs
Dec 2014
Performance Monitoring and Evaluation
Dec 2014
Nordic Treasury: Optimising Funding and Liquidity
Dec 2014
Managing Product Recalls in Accordance with Part 806
Dec 2014
Value Beyond the Pills USA
Dec 2014
Clinical Trial Recruitment Methods and Metrics
Dec 2014
HIPAA Audits in 2015 - What to Expect and How to Prepare
Dec 2014
Contract Law Fundamentals for Non-Lawyers
Dec 2014
Corporate Legal Excellence
Nov 2014
Women in Justice Africa
Nov 2014
ISO 13485 for Medical Devices
Nov 2014
Regulation of Electricity Networks
Nov 2014
Flare Management & Gas Utilization
Nov 2014
CitiesAlive - The Annual Green Roof & Wall Conference
Nov 2014
Annual PPP in Turkey and the Black Sea Conference
Nov 2014
US Regulatory Affairs
Nov 2014
FERPA Policy and Procedure Audit
Nov 2014
Annual Forum on Insolvency and Restructuring
Oct 2014
Ship Air-Emissions Management
Oct 2014
ISO 14971:2012 - Does your current Risk Analysis still comply with your CE Mark requirements
Oct 2014
Contract Law Fundamentals for Non - Lawyers
Oct 2014
Pricing & Reimbursement Strategies for the Russian Market
Oct 2014
Infocast`s Safer Consumer Products Summit
Oct 2014
Lets Get Back to the Basics of Withholding, Depositing and Reporting Federal Taxes
Oct 2014
Regulatory Affairs in Emerigng Markets
Oct 2014
Legacy System Replacement in an FDA-Regulated Environment
Oct 2014
Gas and Petroleum Law Mozambique - Market Briefing (Johannesburg)
Oct 2014
Project and Construction Management Professions Conference
Oct 2014
Global eSubmissions
Oct 2014
Middle East Risk Management Forum
Oct 2014
Preparing for Year End and Year Beginning 2015
Oct 2014
Functions, Procedures and Permits of COFEPRIS & SENASICA - Agencies Regulating Fresh and Processed Foods in Mexico
Oct 2014
IAITL Conference - International Association of IT Lawyers
Oct 2014
Managing Risk in CYBERSECURITY
Oct 2014
Developing a Title IX Compliance Plan
Oct 2014
Implementing the Best Practices for FDA Inspection Preparation and Management
Oct 2014
IT Governance, Risk and Compliance
Sep 2014
Effective Complaint Handling, Medical Device Reporting and Recalls and Avoiding Costly Errors
Sep 2014
Effective Complaint Handling, Medical Device Reporting and Recalls and Avoiding Costly Errors
Sep 2014
Campus Safety`s Role in Title IX Investigations
Sep 2014
Polymers in Drug Delivery
Sep 2014
Marihuana for Medical Purposes
Sep 2014
Anti-Money Laundering Summit
Sep 2014
FX Global Forum@Frankfurt
Sep 2014
FDA Regulations for Food, Drugs, Biologics, Cosmetics, and Medical Devices Including IVDs
Sep 2014
International Symposium on the Forensic Sciences (ANZFSS)
Sep 2014
SOP and FDA Compliance
Aug 2014
Sri Lanka Hospitality Investment Conference
Aug 2014
Law and Politics (BICLP)
Aug 2014
FDA`s and the U.S. Customs Border Patrol`s Import and Export Control Program
Aug 2014
How to handle a regulatory inspection to avoid FDA-483 issues
Aug 2014
Role of Analytical support during various audits - Regulatory and Non Regulatory
Aug 2014
Public Safety and Internal Security Asia
Aug 2014
Analyzing Your Biggest Data - Practical Text Mining for FDA-regulated Companies
Aug 2014
Food Laws and Regulations in Mexico
Aug 2014
Carmel Valley eDiscovery Retreat (CVEDR)
Jul 2014
FERPA Regulation Basics
Jul 2014
Utility Reliability Compliance Forum
Jul 2014
NAFTA Rules of Origin and Documentation
Jul 2014
Annual Government Health Care Congress
Jul 2014
21 CFR Part 11 Add-On Inspections by the FDA
Jul 2014
Litigation Law Clerk Forum
Jul 2014
English Contract Law Course
Jul 2014
Understanding FDA and Avoiding Inspections Leading to Warning Letters, Seizures, Injunctions and Prosecutions
Jul 2014
FDA Guidance Design Considerations for Pivotal Clinical Investigations for Medical Devices
Jul 2014
Annual Conference Regulatory Process Excellence Pharma
Jul 2014
Hemophilia World Asia
Jun 2014
China International New Energy Vehicle Forum
Jun 2014
Conflict Minerals Reporting and Supply Chain Transparency
Jun 2014
Essensials of European Regulatory Affairs
Jun 2014
Structuring and Financing PPP Projects in Africa
Jun 2014
International Symposium on Advances in Legal Medicine (ISALM)
Jun 2014
Annual Global Anti-Corruption Compliance Conference
Jun 2014
Pharmaceutical Regulatory Requirements in Japan
Jun 2014
EU Research & Innovation Master of Finance and Administration
Jun 2014
Postgraduate Diploma/Masters in European Union Law - From King`s College London
Jun 2014
UK, EU and US Copyright Law
Jun 2014
Postgraduate Diploma/Masters in EU Competition Law - From King`s College London
Jun 2014
Computer and Communications Law
Jun 2014
Preparing for FDA BIMO Inspection and Management
May 2014
Annual Forum on Payments Compliance in Canada
May 2014
Controversies around FDA`s Proposed Produce Safety Rules
May 2014
Direct Action Policy Conference
May 2014
EU Research & Innovation Project Management and Financial Reporting
May 2014
Filing Variations
May 2014
Annual Global Gas & LNG Summit
May 2014
International Compliance Professionals Association (ICPA) EU Conference
May 2014
International Annual Conference on Law
May 2014
Valuation Methods (U.S. Customs) for Imports into the United States
May 2014
US-Mexico Real Estate Investment Summit
May 2014
Copyright Considerations for Using MOOCs in Your Courses
May 2014
Meet FDA Expectations for a Tougher Supplier Audit Program
May 2014
The United States Cyber Crime Conference
May 2014
Environmental Claims
May 2014
Business and Operations Guide to Public Procurement - Edmonton
May 2014
Enforcing and Protecting Trade Marks
Apr 2014
Pension Law, Governance and Solvency
Apr 2014
Gulf Conference on Social Responsibility & ISO 26000
Apr 2014
International Real Estate Research Symposium (IRERS)
Apr 2014
Fundamentals of Administrative Law
Apr 2014
Certificate in Trade & Transport Law
Apr 2014
Implementing a Unique Device Identification (UDI) System - Issued on 2013
Apr 2014
European Funding Academy -2020 - Spring Edition
Apr 2014
Risk-Based Approaches to Clinical Trials
Apr 2014
Regulatory Information Management
Apr 2014
Introduction to Regulatory Affiars in the MENA Region
Apr 2014
Foundation Diploma in Admiralty Law & Practice
Mar 2014
Indian Ocean Futures Conference
Mar 2014
Annual Nordic Intellectual Property Rights Forum
Mar 2014
Forex IndustrySummit China
Mar 2014
Regulatory Reform
Mar 2014
International Road Traffic Accident Conference
Mar 2014
Biometrics Summit
Mar 2014
Forensic Investigations to locate and identify the missing
Mar 2014
Child Online Safety and Protection Conference
Mar 2014
Annual Medical Device Directive and the Recast
Feb 2014
China Securitization Summit
Feb 2014
C4ISR Summit
Feb 2014
Regulatory Information Management
Feb 2014
The Inaugural LGBTIQ Conference
Feb 2014
EAR Boot Camp
Feb 2014
Annual European Renewable Energy Project Finance
Feb 2014
Chemical Control and Hazard Communication Regulations
Feb 2014
Medical Design and Manufacturing Executive Summit
Feb 2014
RoHS2 Compliance for Medical Devices
Feb 2014
EU Biosimilar Registration and Marketing Requirements
Feb 2014
International Letters of Credit
Jan 2014
Mental health and stress in the workplace: Guidelines for meeting your accommodation duties
Jan 2014
Arctic Oil & Gas Summit
Jan 2014
Corporate Social Responsibility for the Extractive Industries
Jan 2014
Phacilitate Vaccine Forum Washington
Jan 2014
The boomer generation: Proven solutions for managing an aging workforce
Jan 2014
HSE Med Summit
Jan 2014
FDA Inspection: Preparation and Management
Jan 2014
Non-occupational disabilities: How far must an employer go in accommodation?
Jan 2014
Process Safety Management for the Chem/Petrochem & Refining Industries
Jan 2014
How to Prepare and Submit a Bullet Proof 510(k) and Latest FDA Proposed Changes to the Process
Dec 2013
The Annual International Copyright Law
Dec 2013
Saudi Trade Finance Summit
Dec 2013
Annual Tax Planning for Non-Domiciliaries
Dec 2013
Towards Research Excellence Conference
Dec 2013
Biosimilars - Commercial Strategies and Regulatory Guidelines
Dec 2013
Software Validation for the New FDA Inspections - Electronic Records and Electronic Signatures: From 21 CFR Part 11 to HIPAA
Dec 2013
European VS national energy policy in the light of international energy markets
Dec 2013
2-day In-person Seminar: Why is FDA at my facility, and what do I do during an inspection?
Dec 2013
Asia Summit on Economic Sanctions Compliance and Enforcement
Dec 2013
How to Deal with the IRS and other Governmental Agencies
Dec 2013
Maritime Crime
Dec 2013
Telecoms Cost Accounting & Profitability
Dec 2013
Implementation of eCall
Dec 2013
annual Food Regulations and Labelling Standards Conference
Dec 2013
Annual REGULATORY COMPLIANCE FOR FINANCIAL INSTITUTIONS
Nov 2013
Pharmaceutical Intellectual Property Forum (PIPF)
Nov 2013
Novel Drug Delivery System (NDDS) and Clinical Trial Management China
Nov 2013
Effective Contract Drafting and Advanced Negotiation
Nov 2013
Pension Funds Governance and De-Risking Summit
Nov 2013
Preparing For The Management Occupancy Review (MOR)
Nov 2013
National Advanced Forum on Financial Institutions Insurance
Nov 2013
International Boundary Disputes and Unitization
Nov 2013
International Conference on the Foreign Corrupt Practices Act
Nov 2013
Dubai International Food Safety Conference - DIFSC
Nov 2013
CBP’s Trade Transformation Initiatives
Nov 2013
The Sunshine Act - Have you seen the light?
Nov 2013
School Safety Symposium
Nov 2013
American Conference Institute`s National Rx Drug Pricing Boot Camp
Nov 2013
FDA vs. EU Inspections - How to Prepare and What are the Differences
Nov 2013
Robust Corrective And Preventive Action (CAPA)
Nov 2013
Electric Vehicle Infrastructure China Summit
Nov 2013
Maritime Security Caribbean
Nov 2013
Unique Device Identification (UDI) Final Rules Overview
Nov 2013
Annual FDA Boot Camp Devices Edition
Nov 2013
DCAA Audits
Nov 2013
Thorough and Complete Investigations and Follow-up - A Current Regulatory Expectation
Oct 2013
Legal, Regulatory and Compliance Forum on Over the Counter Drugs
Oct 2013
WrB USA (World Regulatory Briefing)
Oct 2013
Canadian Brownfields : Making Great Places
Oct 2013
Local Government Pension Investment Forum
Oct 2013
Federal Sentencing Guidelines for Organizations (FSGO) Guidelines for your GRC System
Oct 2013
Charging for Investigational Drugs: Current Application of 21 CFR Part 312 and the Expanded Access Rules
Oct 2013
Financial Risk Management
Oct 2013
FERPA: When to Involve Legal Counsel and Leadership
Oct 2013
Effective Discipline and Lawsuit-Proof Termination: How to Remedy Performance and Conduct Problems While Minimizing Your Legal Risks
Oct 2013
Citizenship by Investment and International Residence
Oct 2013
Child Support Garnishments: Withholding Procedures for
Oct 2013
Pharmaceutical and Biotech Patent Strategies & Litigation
Oct 2013
Birth Injuries, The Law & Perinatal Safety
Sep 2013
Energy Infrastructure Investment Summit
Sep 2013
MDiT Forum and Regulation Summit
Sep 2013
Annual National Forum on CLASS ACTIONS LITIGATION
Sep 2013
Environmental Site Assessment (ESA) Phase I and II (1.2 CEUs)
Sep 2013
Pharmaceutical Law Academy
Sep 2013
Annual Advanced FORUM ON PENSION REFORM, LITIGATION AND GOVERNANCE
Sep 2013
Practical Application of the Statutory Residence Test
Sep 2013
The Canadian Institute Advanced Guide to PUBLIC PROCUREMENT
Sep 2013
Annual Construction Law Summer School
Sep 2013
Building an Effective Global Code of Conduct: The Eight Essential Elements of Successful Customization
Aug 2013
Coping with a Difficult Compliance Officer when Responding to a 483, Warning Letter, Import Alert or Recall
Aug 2013
Social Media Law Conference
Jul 2013
Copyright Law: Practical Application and Training
Jul 2013
Oil and Gas Opportunities in Myanmar
Jul 2013
Update on Part 2A
Jul 2013
Medical Device Manufacturing and R&D Summit
Jun 2013
European Summer Academy 2014-2020
Jun 2013
Maximising Pharma Patents
Jun 2013
CPhI China and world medical forum
Jun 2013
Annual International Forum on Policy and Decision Making
Jun 2013
Annual Industrial and Workplace Relations National Conference
Jun 2013
American Bankers Association (ABA) Regulatory Compliance Conference
Jun 2013
New HIPAA Breach Notification Standards - Tougher Rules Require Risk Assessment
Jun 2013
FP7 – Master of Finance and Administration
Jun 2013
OrthoTec Conference
Jun 2013
FP7–Project Management and Financial Reporting
May 2013
Annual PPP in CEE and SEE Summit
May 2013
FDA Warning Letter Closeout Program
May 2013
Litigation and Corporate Counsel Asia Summit
May 2013
International Symposium on Digital Forensics and Security
May 2013
ISDA Master Agreements, CSA & New Documentation for Cleared Swaps
May 2013
Securities Litigation & Enforcement
May 2013
Myanmar Transport & Logistics Summit (MTL)
May 2013
Tax Risk, Strategy & Compliance
May 2013
Promoting and Advertising Dietary Supplements in Compliance with FDA and FTC Regulations: One and a Half-day In-person Seminar
May 2013
Annual International Trade Compliance Conference
Apr 2013
Conducting Successful FDA Meetings to Negotiate Product Development and Approval: 2-day In-person Seminar
Apr 2013
Regulatory Information Management
Apr 2013
Medical Device Labeling (In-Vitro Lab “Home Brew” off - Label Guidance & Enforcement): 2-day In-person Seminar
Apr 2013
EU Energy Shale Gas Conference
Apr 2013
Dietary Supplements - Regulatory Compliance Requirements, Product Claims, Labeling Issues and FDA Updates
Apr 2013
Providing Assurance on GRC Activities
Apr 2013
Dietary Supplements Labeling - Avoiding Claims that Invite Scrutiny and Penalties
Apr 2013
510(k): Format and Contents
Apr 2013
Focus on Internal Control - Is your Company Ready for the New COSO?
Apr 2013
Complaint Handling in Compliance with FDA and ISO Regulations
Apr 2013
ICAGGHR : International Conference on Anti-Corruption, Good Governance and Human Rights
Mar 2013
India Investment Summit
Mar 2013
Microbiological Risk: Do I Really Need to Test Raw Materials for Microorganisms
Mar 2013
The Corporate Director`s Fiduciary Role and Management`s Relationship
Mar 2013
Aerospace + Defense Contract Management Training Forum
Mar 2013
Obtaining Faster FDA 510(k) Approvals - The 510(k) as an Advocacy Document: One and a Half-day In-person Seminar
Mar 2013
International Interuniversity Scientific Conference “Russia & Modern World: Problems of Political Development”
Mar 2013
Legal Issues for Investing in Africa
Mar 2013
FDA Medical Device Approval Process (510(k), IDE, PMA)
Mar 2013
Introduction to the US Department of Justice`s New FCPA Guidance Document - Key Takeaways & Future Planning
Mar 2013
Mexico Investment Summit
Mar 2013
FDA Warning Letters - Stop Fumbling your Response and Effectively Demonstrate Compliance
Mar 2013
Long-Term Care Management for Dual Eligibles Summit
Feb 2013
Process Validation for pharmaceutical and Biopharmaceuticals
Feb 2013
Joint Venture Contracts
Feb 2013
Social Media for Government Communications
Feb 2013
Defining Computer System Validation & Software Development Life-Cycle
Feb 2013
Medicare Advantage Member Accounting & Reconciliation Symposium
Feb 2013
14 CFR Part 21, Subpart K Requirements for Parts Manufacturer Approvals (PMA) - FAA Approval
Feb 2013
Purchasing and Supplier Controls in the Medical Device Industry
Feb 2013
RiskMinds Insurance
Feb 2013
IP and Media in the Digital Age conference
Feb 2013
Conformance of Design History Files for Mature Medical Products
Feb 2013
Directors and Officers (D&O) Liability and Insurance - Everything a New Risk Manager Needs to Know
Jan 2013
Western Aboriginal Consultation & Negotiation
Jan 2013
Derivatives
Jan 2013
Prepaid Card Compliance
Jan 2013
Deviation Management System
Jan 2013
Risk Status Oversight – New Risk Oversight Expectations and Financial Reporting Requirements
Jan 2013
Auditor Independence: Challenges and Opportunities
Jan 2013
The Canadian Institute`s Environmental Law & Regulation in B.C.
Jan 2013
Myanmar Business Conference
Jan 2013
Dual Eligibles Best Practices Summit
Jan 2013
SOX Compliance for Foreign-based Public Companies : Implementing US Corporate Governance and Internal Controls
Jan 2013
Life Cycle of Orphan Drug Development & Commercialization
Jan 2013
`Zero Graffiti` International Conference
Jan 2013
Annual Pricing, Reimbursement & Market Access in Pharma
Jan 2013
National Forum on Prepaid, Gift Cards and Stored Value Products
Dec 2012
Responsible E-cycling/E-waste Management
Dec 2012
FATCA Compliance Conference
Dec 2012
FP7 Financial Management and EC Audits
Dec 2012
Swaps and Derivatives
Dec 2012
Ensuring Integrity and Security of Electronic Records for FDA Compliance
Nov 2012
Obtaining an FDA Investigational Device Exemption - Webinar By GlobalCompliancePanel
Nov 2012
Annual IT For Government
Nov 2012
FDA Guidance Regarding Clinical Trials for Foods, Food Ingredients, and Dietary Supplements
Nov 2012
EC Audits of FP7 in practice - How to get prepared for the inevitable?
Nov 2012
21 CFR Part 11 - Complete Manual for Compliance and Success
Nov 2012
Design Control for Medical Devices
Nov 2012
St. Petersburg cultural forum
Nov 2012
FP7-Project Management and Audits
Nov 2012
The Investigational Medicinal Product Dossier (IMPD): EU CTA vs. FDA IND: Comparing the Content and Agency Expectations
Nov 2012
Avoiding an FDA Warning Letter with a Strong CAPA Program
Nov 2012
eDiscovery for Financial Services
Nov 2012
21 CFR Part 11: Complying with Part 11 Regulation - Understanding the Predicate Rule
Nov 2012
OSHA Ergonomics Compliance - What Every Organization Needs to Know
Nov 2012
FATCA Compliance Solutions
Oct 2012
Annual Forum on PHARMA PATENTS
Oct 2012
Confidential Information and Human Resources
Oct 2012
Annual SECURITIES REGULATION AND COMPLIANCE
Oct 2012
Documentation and Investigative Report Writing
Oct 2012
FP7 Master-class+
Oct 2012
Health Information Privacy and Security Summit
Oct 2012
Harmonized Tariff Schedule and Schedule B
Oct 2012
Canada Documentation and Procedures
Oct 2012
Transforming Risk Management in the Public Sector
Oct 2012
Creating Material, Waste, and Personnel Flow Diagrams for Cleanrooms and Controlled Environments
Oct 2012
Annual Global IP Exchange
Oct 2012
Developing and Maintaining Pre-marketing Master Regulatory Files
Oct 2012
Risk Management: ISO14971, IEC62304 and IEC60601-1: 2005 Compliance
Oct 2012
PS 9000-2011 in the Pharmaceutical Supply Chain - Standards for Pharmaceutical Packaging Materials and Components: New Requirements and Implications
Oct 2012
Live webinar on Auditing Software Vendors & Service Providers for 21 CFR Part 11
Oct 2012
21 CFR Part 11 and Annex 11; What you Need to Know to Pass the New Regulatory Audits
Oct 2012
Annual UK Ports National Conference
Sep 2012
Title IV: Complying with New State Authorization Rules
Sep 2012
HITECH - Why It`s Important to Comply Now
Sep 2012
The New HIPAA Audit Protocol - What It Takes To Be Ready For An Audit
Sep 2012
Medical Device Regulations in Europe
Sep 2012
The OTC Derivatives Summit
Sep 2012
China Intellectual Property Focus (CIPF2012)
Sep 2012
Optimizing Regulatory Communications and Submissions
Sep 2012
Asia Pacific Chapter FBINAA Conference
Sep 2012
FMEA and Risk Management for Medical Devices
Sep 2012
21 CFR Part 11: How to Successfully Prepare for and Host an FDA Inspection
Sep 2012
Impact of the New Pharmacovigilance Legislation - Key Industry and Regulatory Perspective
Sep 2012
Hazard Analysis – A practical guide
Sep 2012
Transatlantic Regulatory Compliance for Investing Funds
Sep 2012
managing Regulatory and Legal Issues in Shale Plays
Sep 2012
Incorporating Six Sigma DMAIC into CAPA
Sep 2012
Key Steps to Avoid 483 Warning Letters & Remediation if you get one
Sep 2012
Managing for Outcomes: Policy and Program Impact Essentials Masterclass
Sep 2012
Annual eDiscovery West Summit
Sep 2012
International Conference on Bioethics Education: Contents, Methods, Trends
Sep 2012
(QMS) Competence and Training Requirements per FDA QSR and ISO 13485
Aug 2012
Validation and Use of Excel Spreadsheets in Regulated Environments - Webinar By GlobalCompliancePanel
Aug 2012
Site Challenges in Conducting Investigational Device Trials
Aug 2012
Canadian International Trade Compliance
Aug 2012
Essential Policy Skills - Training Series
Aug 2012
Preventing, Documenting, and Dealing with FMLA Abuse
Aug 2012
Service Rig Move - National Safety Code Standard 9
Aug 2012
Changes to Good Pharmacovigilance Practices in the EU - Webinar By GlobalCompliancePanel
Aug 2012
Regulatory Complaint Handling, MDR`s & Recalls - Webinar By GlobalCompliancePanel
Aug 2012
Common Sense Water System Validation - Webinar By GlobalCompliancePanel
Aug 2012
Maximizing ROI on Each Compliance Effort - Webinar By ComplianceOnline
Jul 2012
One and a Half-day In-person Seminar: FDA Compliant GLP for Nonclinical Studies - For Pharmaceutical and Medical Device Industries
Jul 2012
Strategic Selection and Development of Immunogenicity Binding Methods
Jul 2012
Auditing GRC Programs - Webinar By ComplianceOnline
Jul 2012
World Congress on Risk
Jul 2012
Annual SOX/ for Insurance Conference
Jul 2012
What Every FDA Regulated Company Needs to Know About its FDA District Office
Jul 2012
Managing the PIP in Drug Development
Jul 2012
FDA’s Regulation of Veterinary Regenerative Medicine
Jun 2012
Information Management and Governance for the Public Services
Jun 2012
Anti-Corruption & Bribery Compliance
Jun 2012
Annual Regulatory Compliance in Energy Trading
Jun 2012
BC Aboriginal Consultation & Accommodation
Jun 2012
The Fundamentals of Aboriginal Law
Jun 2012
Condominium Congress
Jun 2012
Annual Regulatory Cost Modelling & Accounting
Jun 2012
Navigating the Japan and South Korean Regulatory Compliance and Clinical Trial Environment
Jun 2012
Fundamentals of Nuclear Power
Jun 2012
Annual Orphan Drug Congress
Jun 2012
World Economic Forum on the Middle East, North Africa and Eurasia
Jun 2012
Service Level Agreements (SLAs) - Preparation Guidelines for Effective SLAs - Webinar By ComplianceOnline
Jun 2012
Election Year Legal and Compliance - Webinar By ComplianceOnline
May 2012
IP Due Diligence in Corporate Transactions
May 2012
Incoterms Rules
May 2012
FIMA REGULATION
May 2012
Unfair Commercial Practices and Consumer Protection
May 2012
Prisons and Correctional Facilities Asia
May 2012
Edition SOX Compliance & Evolution to GRC
May 2012
EU FUNDS FOR ROMANIAN ORGANISATIONS
May 2012
Import Compliance - How to Reduce Your Import Risks
May 2012
International Terms 2010 Rules By Compliance2go
May 2012
Improving Bank Compliance Management
May 2012
Nano Aqua
May 2012
IT Risk Management – EU Laws and Regulations
May 2012
Equipment Calibration in FDA QSR – Regulations and Warning Letters
May 2012
EC Financial Audits: Get prepared for the inevitable!
May 2012
FP7 Financial Management and Reporting
May 2012
FP7 Technical Management and Reviews
May 2012
Proper Documentation of Risk Management for Compliance with ISO 14971 - Webinar By GlobalCompliancePanel
May 2012
Applying GMP Quality Principles To Establish A Reduced Testing Program
May 2012
Physician Payment Sunshine Act and State Sunshine Law Compliance. Are you Prepared for the New Federal Requirements and Existing State Requirements?
Apr 2012
DHF, DMR, DHR and TF - Regulatory Documents Explained, and Best Practices for Controlling Them
Apr 2012
How to Survive FDA`s `New` Inspection and Enforcement Practices
Apr 2012
Personal Injury Law
Apr 2012
Patent Validity and Infringement
Apr 2012
Lean Project Management For U.S. FDA-Regulated Industries
Apr 2012
Law and Technology: Innovation in the Digital Age - A World Jurist Association (WJA) conference
Apr 2012
Complying with the EU Cookies Law Ecosystem
Apr 2012
The CLA Regional Law Conference
Apr 2012
Texas Criminal Justice Information User Group Conference
Apr 2012
Horizon 2020 and FP7- A practical perspective
Apr 2012
International Sanctions in the Energy Industry
Apr 2012
Class Actions Litigation Bootcamp
Apr 2012
World Pharma Trials Congress LatAm
Apr 2012
World Generic Congress LatAm
Apr 2012
BioPharma LatAm Convention
Apr 2012
Hostage: Prevention and Response
Apr 2012
Preparing for MHRA Pharmacovigilance Inspections
Apr 2012
Acceptance Activities in FDA QSR - Regulations and Warning Letters
Apr 2012
World Vaccine Trials Congress
Apr 2012
Good Documentation Practices for GXPs
Apr 2012
Making Risk-Benefit Decisions – Preparing for the New FDA Guidance Documents
Apr 2012
Comprehensive Course on RECORDS RETENTION
Apr 2012
Post Macondo – New Safety, Environmental, Commercial Implications for Offshore Oil & Gas in the EU and beyond
Apr 2012
Novel Pricing and Market Access Strategies
Apr 2012
California Environmental Regulations – Differences Between Federal EPA and State Requirements
Apr 2012
Medical Device Risk Management Using ISO 14971
Mar 2012
World Congress on Healthy Ageing - Evolution: Holistic aging in an age of change
Mar 2012
Master Verification & Validation Planning under U.S. FDA CGMP, ICH Q-series and ISO 13485-14971 Requirements - Webinar By GlobalCompliancePanel
Mar 2012
Live webinar on Latin America: Regulatory Compliance Requirements for Life Science Products (Focus: Brazil, Mexico, Argentina) By Compliance2go
Mar 2012
Forensic Investigation and evidence handling
Mar 2012
Phacilitate Leaders` Forum West
Mar 2012
Changes in the EU Medical Device Directives; 2010 Modifications and the Recast of the MDD Directives - Webinar By GlobalCompliancePanel
Mar 2012
Reduce the Risks of Foreign Material Contamination - A Manufacturer`s Guide in Creating a Foreign Material Control
Mar 2012
How to Develop, Monitor and Effectively Communicate your Risk Control Strategy - Webinar By GlobalCompliancePanel
Mar 2012
Insurance Distribution Forum
Mar 2012
Webinar: When Do You Need a 510K?
Mar 2012
Medical Device Adverse Event Reporting and Vigilance System During Clinical Trials and Post-Marketing: US, EU, and Canada
Mar 2012
Managing Party & Counterparty Relationship Risks
Feb 2012
The Canadian Institute’s Decision Writing & Running a Fair Hearing
Feb 2012
Litigation Asia Summit
Feb 2012
ITC Litigation & Enforcement
Feb 2012
Defending Against an OFAC Investigation
Feb 2012
Seaport Security Asia
Feb 2012
Gaming Executive Summit LatAm - GES
Feb 2012
Implement a Tougher Supplier Audit Program - Webinar By GlobalCompliancePanel
Feb 2012
The Canadian Institute’s 8TH ADVANCED GUIDE TO PUBLIC PROCUREMENT
Feb 2012
Dietary Supplement Regulatory Compliance in the United States: Labeling, Product Claims & Updates from the FDA - Webinar By GlobalCompliancePanel
Feb 2012
National Derailment Investigations Workshop
Feb 2012
Annual Payment Card Compliance
Feb 2012
FATCA
Feb 2012
Incident & Accident Investigation
Feb 2012
Corporate Governance in CEE & Turkey
Feb 2012
Market Access and Healthcare Reform
Jan 2012
The EU Cosmetics Directive and the new Cosmetic Regulations
Jan 2012
Clear as Mud: Obtaining & Marketing your 510(K) with Today`s FDA
Jan 2012
Importing into the United States in Compliance with U.S. Customs & Border Protection (CBP)
Jan 2012
Sante et Securite au Travail
Jan 2012
ADVERSE EVENT MANAGEMENT DURING MEDICAL DEVICE CLINICAL STUDIES IN EUROPE
Jan 2012
Validation and use of Access Databases in FDA regulated environments
Jan 2012
Regulation
Jan 2012
Record Keeping for a (Food) Recall: Keeping Records to Minimize the Affect of a Recall
Jan 2012
Anti-Corruption-Munich
Jan 2012
New Dietary Ingredients in the Regulatory Scheme
Jan 2012
Middle East Summit on Anti-Corruption
Jan 2012
Fraud and Asset Tracing Gulf
Jan 2012
Trial Master File Summit
Jan 2012
FDA’s New Food Safety Law - What does It mean for everyone in the Global Food Chain
Jan 2012
Cyber Security for Government Asia
Jan 2012
An Introduction to the FDA New Drug Approval Process
Jan 2012
Introduction to FDA Good Documentation Practices
Jan 2012
Nano Health
Jan 2012
Australian Accountants & Lawyers Conference
Jan 2012
The International Conference on Economic Management and Information Engineering Technology
Dec 2011
FDA Compliant Handling of Out of Trend Results in Pharmaceutical Quality Control
Dec 2011
Accounting of Disclosures under HIPAA: What the Rules Require Today and What`s Changed by the Proposed Rule
Dec 2011
The Annual Telecommunications Law & Regulations in the Middle East Conference
Dec 2011
Live webcast on HOW TO MANAGE COMPLAINT FILES by Compliance2go
Dec 2011
Infrastructure Investment World India
Dec 2011
GMP Annual Training
Dec 2011
Brazil Investment Summit UK
Dec 2011
Mongolia Investment Summit
Dec 2011
Corporate Compliance & Risk Management Excellence
Dec 2011
FDA MEDICAL DEVICE INSPECTIONS - Are You Prepared?
Dec 2011
Live webinar on Excel Spreadsheet Compliance with 21 CFR 11 by Compliance2go
Dec 2011
Site feasibility and study start up
Dec 2011
Biocompatibility Testing and Evaluations for Medical Devices
Dec 2011
Sustainable Construction Qatar
Dec 2011
Electricity Market Reform: the White Paper and beyond
Dec 2011
Ship Arrest – Where and how to arrest a ship
Dec 2011
Planning for Global Registrations
Dec 2011
Operational and Technical Challenges for Arctic Shipping Seminar
Dec 2011
THE PRACTICE OF ORAL PROCEEDINGS AT THE EUROPEAN PATENT OFFICE
Dec 2011
eDiscovery Readiness for Government
Dec 2011
Investment Adviser Compliance Forum
Dec 2011
Foundation Diploma in Time Charterparties
Dec 2011
Foundation Diploma in Tanker Charterparties
Dec 2011
Canadian Anti-Spam Legislation: Understanding the Requirements and Ensuring Compliance – An In-Depth Look (Workshop)
Dec 2011
THE NEW ISO 14155 REQUIREMENTS FOR MEDICAL DEVICE CLINICAL STUDIES
Dec 2011
Tariff Policies, Models and Methods
Nov 2011
Navigating 510(k) and PMA Submissions and Approvals
Nov 2011
THE DEVELOPMENT SAFETY UPDATE REPORT (DSUR)
Nov 2011
Russia: The inside story
Nov 2011
Document Approval, Control, and Distribution: How to Develop a Compliant, Cost Effective System By Compliance2go
Nov 2011
THE BORDERLINE BETWEEN MEDICINES AND FOODS
Oct 2011
UrbanTec
Oct 2011
Draft Guidance for Device Industry and FDA - Postmarket Surveillance - Webinar By GlobalCompliancePanel
Oct 2011
World Economic Forum on the Middle East
Oct 2011
Introduction to Regulatory Affairs for Biotech
Oct 2011
FP7-Autumn Academy
Oct 2011
Kommunale
Oct 2011
Does your Equipment Program Meet Current Regulatory Expectations - Webinar By GlobalCompliancePanel
Oct 2011
Live webinar on The FDA Inspection: Preparation, Performance, and Follow-up by compliance2go
Oct 2011
REGULATORY REQUIREMENTS FOR CLINICAL TRIALS - Including an Update on the Proposed Changes to the Clinical Trial Directive Requirements
Oct 2011
Live webinar on HIPAA and EHRs - what your systems need to do so you can be in compliance with new rules by compliance2go
Oct 2011
FDA`s Draft Guidance on Financial Disclosure by Clinical Investigators - Webinar By GlobalCompliancePanel
Oct 2011
FDA ADVERSE EVENT REPORTING FOR PHARMACEUTICALS
Oct 2011
Effective Internal Auditing-Making Quality Systems More Efficient for the Medical Products Industry - Webinar By GlobalCompliancePanel
Oct 2011
FDA GMP REQUIREMENTS FOR PHARMACEUTICALS
Oct 2011
Risk Management during device design according to ISO14971 - Webinar By GlobalCompliancePanel
Oct 2011
India Energy
Oct 2011
SUCCESSFUL MEDICAL WRITING - Intensive Practical Course
Sep 2011
Regulatory Affairs for Preclinical Safety Studies
Sep 2011
How to Identify Hazardous Wastes at the Work Place - Webinar By ComplianceOnline
Sep 2011
Annual Environmental Product Development Excellence
Sep 2011
Hybrid Quality Systems For Pharmaceuticals - Combining ICH Q7A & Part 210-211 - Webinar By GlobalCompliancePanel
Sep 2011
TAK-Response
Sep 2011
REGULATORY AFFAIRS FOR SUPPORT STAFF ~ PART 2
Sep 2011
Corporate Counsel Exchange Asia Pac
Sep 2011
The Eu Cosmetics Directive And The New Cosmetics Regulations
Sep 2011
The Darker Side of Implementing Wellness Programs: Possible Career-Ending Decisions
Sep 2011
Good Laboratory Practice Regulations: Introduction and Strategies for Implementation
Sep 2011
A Guide to HACCP Validation and Verification for Food Manufacturers and Restaurants
Sep 2011
Medical Device Regulations In Asia Pacific Market
Sep 2011
HIPAA Audits and Enforcement - new rules, new penalties, and a new audit program
Sep 2011
Accelerating IP and Innovation in South Africa
Sep 2011
HIPAA Security Policies and Procedures: What you Need for Compliance
Sep 2011
Practical Ensuring Compliance and Fighting Frauds in Russia and CIS
Sep 2011
FDA Validation Requirements - Webinar By ComplianceOnline
Sep 2011
Drug Master Files - Understanding and Meeting your Global Regulatory and Processing Responsibilities
Sep 2011
Annual Pricing and Reimbursement Conference
Sep 2011
Regulation of printing inks on food contact packaging materials in the US & EU
Sep 2011
A Rational Approach to Developing and Troubleshooting Dissolution Methods for a Variety of Purposes
Sep 2011
Investigator responsibilities and Legal commitments in Drug and Device Clinical Research
Sep 2011
Drug Master Files (DMFs) - Understanding and Meeting Your Global Regulatory and Processing Responsibilities By compliance2go
Sep 2011
Applying GMP Quality Principles to Deviations & Nonconformities and Effective Corrective And Preventive Action Systems
Sep 2011
Reliability Engineering Fundamentals for Medical Devices - Webinar By ComplianceOnline
Sep 2011
Ensuring Integrity and Security of Laboratory Data
Sep 2011
How to design A CAPA System that meets Compliance Requirements
Sep 2011
Nanomaterials: Risks, Regulations & Rewards
Sep 2011
European Chemicals Policy
Sep 2011
Eliminate the Confusion – Physician Quality Reporting System for Anesthesia Claims
Sep 2011
Responding to FDA Form 483s and Warning Letters - Webinar By ComplianceOnline
Sep 2011
Why Nobody Believes the Numbers: The Secrets of Care Management Outcomes Measurement Revealed
Sep 2011
Master Validation Planning
Aug 2011
Common GCP Violations and Site Mistakes - How to Avoid them
Aug 2011
Effective Hazard Analysis to meet FDA and ISO13485:2003 Risk Management Requirements
Aug 2011
Design, Planning and Conducting Effective Audits
Aug 2011
Risk Analysis Without Fear: Satisfying HIPAA & Meaningful Use Requirements for Privacy and Security
Aug 2011
Device Master Record & Device History Record
Aug 2011
Design History File (DHF) Device Master Record (DMR) Device History Record (DHR) and Technical File (TF) - Regulatory Documents Explained
Aug 2011
Preparing for an FDA Pre-Approval Inspection - Webinar By ComplianceOnline
Aug 2011
A Simpler Approach to Implementing or Validating CGMPs to 21 CFR 11, Electronic Records, Signatures
Aug 2011
Why Post-market Pharmacovigilance trials are increasingly seen : What do they tell us and why are they important
Aug 2011
Design Reviews for Efficiency and Efficacy - Webinar By ComplianceOnline
Aug 2011
Full Day Virtual Seminar: Predicting Product Life Using Reliability Analysis Methods
Aug 2011
How Due Diligence in Accurate Adverse Event Reporting is the Key to a clean FDA Audit
Aug 2011
Understanding the Difference: HIPAA Security Compliance Assessment v. HIPAA Security Risk Analysis
Aug 2011
Sterilization Options for Challenging Products - Webinar By ComplianceOnline
Aug 2011
How to Survive a DEA Inspection Series: Only Manufacturers and Distributors
Aug 2011
ISO 13485 and medical device quality systems - practical strategies for planning, implementation and beyond
Aug 2011
Food Allergen Programs - Current Trends, Technologies and Risk Mitigation
Aug 2011
How to write Standard Operating Procedures (SOPS) & Work Instructions (Wis) that Meet and Exceed Compliance Requirements
Aug 2011
Clinical Project Management - Webinar By ComplianceOnline
Aug 2011
Health Ingredients
Aug 2011
Review and Implementation of USP <1058> Analytical Instrument Qualification
Aug 2011
Design History Files, Device Master Records, Device History Records, and Technical Files / Design Dossiers
Aug 2011
Vendor Qualification - Designing and Implementing an Efficient and Compliant Vendor Program
Aug 2011
360 Degree Approach to Health Information Privacy - Webinar By ComplianceOnline
Aug 2011
Trial Master File for Research Sites: Can You Pass FDA Inspection?
Aug 2011
Auditing the QC Microbiology Laboratory for FDA Compliance - Webinar By ComplianceOnline
Aug 2011
Information Security and Payment Card Rules: Complying with PCI and HIPAA, and Protecting Patient Payment Data
Aug 2011
Bioanalytical Methods Validation - Webinar By ComplianceOnline
Aug 2011
Analytical Test Methods Validation: FDA, ICH and USP Requirements - Webinar By ComplianceOnline
Aug 2011
Full day Virtual Seminar on Pharmaceutical Stability - Webinar By ComplianceOnline
Jul 2011
How to manage an EPA inspection - Webinar By ComplianceOnline
Jul 2011
Vendor Qualification Auditing for FDA Computer System Compliance - Webinar By ComplianceOnline
Jul 2011
Clinical Document Management and Collaborative Electronic Data Exchange in Clinical Trials
Jul 2011
The Investigational Medicinal Product Dossier (IMPD): EU`s CTA vs. FDA`s IND
Jul 2011
Advertising and Promoting FDA Regulated Products - Webinar By ComplianceOnline
Jul 2011
Full-day Virtual Seminar: IND Applications for the US FDA
Jul 2011
How to Avoid the Environmental Compliance Nightmare - Webinar By ComplianceOnline
Jul 2011
Cal/OSHA Enforcement and Defenses – Recent Changes in the Law
Jul 2011
Document Approval, Control, and Distribution: How to Meet FDA QSR and ISO 13485 Requirements
Jul 2011
Using the USP Effectively - Webinar By ComplianceOnline
Jul 2011
How to Meet HIPAA-HITECH Encryption Requirements - Webinar By ComplianceOnline
Jul 2011
Key Concepts in OSHA Recordkeeping – 2.5 hrs comprehensive webinar
Jul 2011
Validation of Analytical Methods and Procedures - Webinar By ComplianceOnline
Jul 2011
Eliminate the Confusion - Compliance for Anesthesia Services
Jul 2011
Procurement Strategies for the Public Sector
Jul 2011
Use of Force Reporting
Jul 2011
Smart Grid Cyber Security Asia Pacific
Jul 2011
Aviation Outlook China
Jul 2011
Life Sciences Strategies for Anti-Corruption & FCPA Compliance
Jun 2011
Navigating the new FDA world of Combination Products
Jun 2011
Master Production Record Requirements - Webinar By GlobalCompliancePanel
Jun 2011
Annual Antitrust and Competition Law
Jun 2011
Russian Real Estate Summit
Jun 2011
Produced Water Treatment
Jun 2011
Preparing the Chemistry and Pharmacy Section of the EU Registration Dossier
May 2011
Freedom of Information
May 2011
Customs Compliance in Russia & CIS
May 2011
Strategies for the Planning, Design and Security of PRISONS & CORRECTIONAL FACILITIES ASIA
May 2011
PHARMACEUTICAL WATER EDINBURGH
May 2011
India Summit on Anti-Corruption
May 2011
National Conference on the FCPA and Anti-Corruption for the Life Sciences Industry
May 2011
KIHE
May 2011
Post-Market Drug Safety Forum
May 2011
Transmissible Spongiform Encephalopathies
May 2011
Information Retention & E-Disclosure Management Europe
May 2011
Construction Law
May 2011
Turkey Investment Summit
May 2011
FDA Clinical Trial Auditing and the due diligence Companies should conduct as part of their monitoring program - Webinar By GCP
May 2011
Regulatory Compliance Risk
May 2011
Information Security Risk Analysis: Meeting HIPAA Requirements and the Meaningful Use Objective - Webinar By GlobalCompliancePanel
May 2011
Avoiding `Failure to Investigate` - Observations by Conducting Effective Investigations
Apr 2011
How to successfully create a Device History Record and keep FDA happy in the process - Webinar By GlobalCompliancePanel
Apr 2011
The 510(k) Process and Risk Management
Apr 2011
Data Security Analysis for Healthcare Providers - Webinar By GlobalCompliancePanel
Apr 2011
Legal Week Future of Legal Services Forum
Apr 2011
China Summit on Export Controls
Apr 2011
US-FDA Drug Submission Procedures
Apr 2011
Government Contract Cost & Pricing
Apr 2011
Vendor/Supplier/CRO Compliance – Lessons Learned & Rules to Live By
Apr 2011
WJA Mauritius Conference
Apr 2011
The International Conference – Gateway to Africa
Apr 2011
Combination Products
Apr 2011
Government Construction Contracs and Compliance
Mar 2011
European Regulatory Affairs School
Mar 2011
What Health Reform (and other Recent Changes) Means for Corporate Compliance
Mar 2011
Corporate Counsel Summit
Mar 2011
Treasury for Tax People
Mar 2011
Westminster Legal Policy Forum Keynote Seminar: Libel law - the next steps
Mar 2011
Process Validation: current industry practices and FDA Guidance Document Review - Webinar by GlobalCompliancePanel
Mar 2011
Eastern Claims Conference
Mar 2011
How to prepare for Increased OSHA penalties in
Feb 2011
Last changes in Canadian ethics regulations for clinical trial
Feb 2011
Permanent Establishment Mastercourse
Feb 2011
Landed Estates: Tax Planning & Wealth Preservation
Feb 2011
Legal Week Audience with... IT directors
Feb 2011
Iraq and Afghanistan Contracting
Feb 2011
ITAR Boot Camp
Feb 2011
Westminster Legal Policy Forum Keynote Seminar: `A rehabilitation revolution?` - next steps in skills and resettlement for offenders
Feb 2011
Understanding the Technical Requirements of 21 CFR Part 11 - Webinar by GlobalCompliancePanel
Feb 2011
Don`t RISK to ignore RISKS. Understanding ISO 14971
Feb 2011
Advanced Debt Collections and Recovery
Feb 2011
Export Controls
Feb 2011
Understanding and Implementing FDA’S 21 CFR Part 11
Feb 2011
Westminster Legal Policy Forum Keynote Seminar: The legal aid system - proposals for reform
Feb 2011
Nuclear New Build
Jan 2011
The Life Sciences Lawyer`s Guide to
Jan 2011
Anti-Corruption, Frankfurt Edition
Jan 2011
Westminster Legal Policy Forum Keynote Seminar: Tackling anti-social behaviour and creating active communities
Jan 2011
Western Canada ABORIGINAL LAW FORUM
Jan 2011
C5’s European Tank Storage Summit
Jan 2011
Clinical Trials
Jan 2011
Fraud, Asset Tracing and Recovery in the Gulf
Jan 2011
cGMP: Strategies for implementation and compliance for Phase I Investigational Drug and Biologic products
Jan 2011
Advertising & Marketing Law
Jan 2011
OTC Derivative Reform & Counterparty Risk
Jan 2011
The basic principles of Islamic Economy and Law
Dec 2010
NCMA`s Annual Government Contract Management Conference
Dec 2010
The Sweet & Maxwell Current Issues in Insolvency Conference - Cutting Edge Developments in Insolvency Law
Dec 2010
NWEC
Dec 2010
Annual Fraud and AntiCounterfeiting Conference
Dec 2010
Preparing for a GSA Audit - ComplianceOnline GSA Webinar
Dec 2010
Real Estate Investment World USA
Dec 2010
Government Contracting Review and 2011 Outlook
Dec 2010
Legal Strategy Forum
Dec 2010
Westminster Legal Policy Forum Keynote Seminar: The future of sentencing policy - short term sentences and reducing re-offending
Dec 2010
NALC Larger Councils’ Conference and Exhibition
Dec 2010
The multinational scopes of US and EU export controls and economic sanctions laws - ComplianceOnline Trade And Logistics Webinar
Nov 2010
Westminster Legal Policy Forum Keynote Seminar: Next steps for improving offender health - following up the Bradley recommendations
Nov 2010
Westminster Legal Policy Forum Keynote Seminar: The future of the legal aid system - challenges, priorities and finance
Nov 2010
FIDE Congress
Nov 2010
Health Technology Assessment Conference - Building a new System to get Effective Treatment to European Patients
Nov 2010
Finance Leaders Forum, 'How the New Financial Legislation Will Impact You and Your Business'
Nov 2010
Westminster Legal Policy Forum Keynote Seminar: Intellectual property, innovation and the UK economy
Nov 2010
40 years of work on standardization at the UNECE
Nov 2010
Oil and Gas Governance Ethics and Compliance
Oct 2010
Annual Antitrust and Competition Law Compliance
Sep 2010
Reducing Legal Risks in the Sale & Marketing of Medical Devices
Apr 2010
Advanced Guide to Alberta`s New Rules of Court
Apr 2010
Bringing and Defending Litigation Against the Crown
Apr 2010
The Commonwealth Regional Law Conference
Apr 2010
GovSec U.S. Law Conference & exposition
Mar 2010
ABORIGINAL LAW and ECONOMIC
Feb 2010
The Conference on The Use of Force in Law Enforcement
Jan 2010

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