Meet Representatives of the Belgian Agency, FAMHP

Meet Representatives of the Belgian Agency, FAMHP
Members of the TOPRA IN Benelux Community Steering Group are pleased to invite you to a webinar during which representatives of the Belgian Federal Agency of Medicines and Healthcare Products (FAMHP) will present the current organisation and the key activities on which the Agency is focussing in line with its strategic business plan. The webinar will cover the key three divisions of the Agency: Directorate General (DG) Pre-Authorisation, DG Post-Authorisation and DG Inspection.



Date: Tuesday 13 May 2025
Time: 12:00 - 13:00 BST 13:00 - 14:00 CET


Benefits for participants

This is a unique opportunity to meet representatives from the Agency and hear updates on how it is organised, what its historical and new spearhead areas are and what its core activities and contributions in a European context are. And this with an opportunity to ask questions.

In this webinar, we will specifically cover:

          - The three divisions (Directorate General) of the FAMHP Organisation
          - It’s core activities in the areas of human and veterinary medicinal products as well as in medical devices.
          - The spearhead areas and strategic business priorities of the Agency



Presenter(s)

Ann Verhoye, Staff Co-worker, FAMHP
Christophe Debruyne, Management Support Co-ordinator DG Inspection, FAMHP
Sara De Clercq, Management Support DG Post Authorisation, FAMHP
 
The session will be facilitated by Frank Vandendriessche and Paula van Hennik as co-chairs of the TOPRA IN BeNeLux Community Steering Group


Frank Vandendriessche is a Pharmacist with PhD and has been active in scientific and strategic regulatory affairs from more than 25 years at three major companies (Pfizer AH, GSKBiologicals, MSD) and as a regulatory affairs consultant for 10 years.



Paula van Hennik has a background as a scientist with a PhD in Haematology and has been active in the field of (clinical) regulatory affairs for 14 years with experience as a regulator (11 years at the Medicines Evaluation Board) and since 2 years as a consultant. 


The main webinar presentation will run for approximately [50] minutes, which will then be followed by a Q&A session.


PRICING
TOPRA Members: Free 
Non-member: £45
When
13/05/2025 12:00 - 13:00
Where
ONLINE
Sign in or create an account to register Registration ends 12/05/2025 16:00 (GMT Daylight Time)
My registration status: Not registered
Your company name
Your VAT country
Your VAT number
NOTE
Important instructions before booking - If your company name or VAT number does not appear here or you would like to be invoiced using a different VAT number, please email finance@topra.org

Register now