Procedures, dossier requirements, pharmacovigilance, policy
Marketing authorisation, reporting adverse events, production, distribution
Our story, our work, the organisation, working at the MEB, contact
08-07-2025 | 11:00
The moment at which new slots become available in the MEB planning tool- used by companies to reserve a timeslot for submitting ...
27-05-2025 | 11:00
The European Medicines Agency (EMA) published a new version of the QRD template in November 2024: QRD template version ...
20-05-2025 | 16:30
The MEB has a new Science Policy for 2025-2029. Four key themes will guide regulatory science at the MEB for the coming four ...
15-05-2025 | 17:00
Starting this year, the Veterinary Medicinal Products Unit (VMPU) will publish the reports of veterinary GMP inspections. The ...
01-05-2025 | 12:00
As of 1 July 2025 it will be mandatory to use the MEB planning tool to reserve a time slot for submitting an application for ...
18-02-2025 | 10:00
Join us for the MEB Science Day 2025, a unique opportunity to share knowledge and connect with colleagues in the field of ...