Variations to Marketing Authorisations is a course dedicated to the EU system for variations, with practical advice on the preparation and submission of variation applications using the various European procedures.
Variations to Marketing Authorisations covers topics such as:
- How pharma companies are working in this evolving regulatory environment
- The EU system for variations
- The impact of Module 3 on your variations dossier
- The preparation and submission of variation applications
- Filing tips and strategies to help achieve faster approval
Variations to Marketing Authorisations brings together:
- Anyone with an involvement in the variations process including clinical safety, QA and pharmacovigilance
- Those working in registration and regulatory affairs
Variations to Marketing Authorisations will be held on 01-02 Feb 2024.
