Date
- Tuesday, 07 May 2024, 10:00 (CEST) - 11:00 (CEST)
Location
- OnlineEuropean Medicines Agency, Amsterdam, the Netherlands
Event summary
Centrally Authorised Products (CAPs) data that is now available in the web-based electronic Application Form (eAF). EMA is hosting this information and Q&A session to explain and showcase the changes in the product data in the web-based Human Variations eAF.
Participants will have the opportunity to ask questions in the last part of the session.
Participation is recommended to industry stakeholders working on regulatory affairs of their respective organisations.
Registration
Registration is open at this link.