Process Validation with Qualification is a conference dedicated to the EU and FDAProcess Validation Guidance.
Process Validation with Qualification covers topics such as:
- Quality Risk Management
- Science and Risk Based Approach to Process Validation for Pharmaceutical and Biopharmaceutical Products
- EU Process Validation Guideline
- FDA Process Validation Guidance
- Lifecycle Approach to Process Validation
- EU Draft Annex 15
- Equipment and Utility Qualification
- Process Design
- Continued Process Verification/Ongoing Process Validation
- Process Performance Qualification/Process Validation
- Process Improvement
- Continued Improvement and Process Optimisation
- Business Benefits
- Implementation Challenges
Process Validation with Qualification brings together:
- Manufacturing attendees
- Development personel
- Quality managers
- Engineers
- Pharmaciss
- Process Engineers
- Quality Assurance Professionals
- Scientists
- Late Stage Product and Process Development Engineers, Scientists, Pharmacists
- Quality Control Managers
- Validation and Qualification Managers
- Technology Scale up and Transfer Managers
- Risk Management Specialists
- Validation and Qualification Specialists
- Operation Managers, Engineers
- Lean management Specialists
Process Validation with Qualification will be held on 21-22 May 2024.
