This webinar will cover the current status of the Post-Market Surveillance (PMS) framework and the upcoming steps required to meet European Medicines Agency (EMA) deadlines.
The session will also address data quality in relation to PMS and the Extended Application Form (eAF), highlighting common challenges and best practices.
In addition, we will present the digital tools and solutions offered by Asphalion to support these activities and facilitate regulatory compliance.
Finally, the webinar will provide an overview of the EMA roadmap and discuss the latest regulatory updates and developments relevant to PMS and related processes.
- Stay Ahead of Upcoming EMA Deadlines
- PMS data review directly impacts the completion of the eAF
- Asphalion can help you review your company’s portfolio data using the digital tools it has developed, ensuring data quality and supporting efficient regulatory compliance.
The webinar will be led by Asphalion expert Sonia Tejeda
📅 1 October- 3:00 p.m. (CET)
🔗 Register now and save your spot: https://bit.ly/4zo0AfT
Contact us for further information: [email protected]
