This third session on the “Sources of life sciences regulation” is intended to provide the participants with a high-level overview of the pharmacovigilance legislation in the European Union and will include a specific part on the Belgian legislation.

Program: 

• 13h00 - Introduction by Joelle Ameye, Pharmacovigilance Manager and Local Safety officer at Teva Pharma Belgium
• 13h05 - Overview of the pharmacovigilance legislation in the European Union and in Belgium by Debby Bollen, Safety & Regulatory Affairs officer at Infarama
• 13h50 - Q&A