Questions and answers on implementation of the medical devices and in vitro diagnostic medical devices Regulations ((EU) 2017/745 and (EU) 2017/746)
PSUSA/00002229/202404
EMEA-001434-PIP01-13-M03
PSUSA/00010774/202403
List of European Union reference dates (EURD) and frequency of submission of periodic safety update reports (PSURs)
Human medicines European public assessment report (EPAR): Vumerity, diroximel fumarate, Date of authorisation: 15/11/2021, Revision: 8, Status: Authorised
Executive Steering Group on Shortages and Safety of Medicinal Products (MSSG) meetings
Human medicines European public assessment report (EPAR): Penbraya, Meningococcal groups A, C, W, Y conjugate and group B vaccine (recombinant, adsorbed), Date of authorisation: 14/11/2024, Status: Withdrawn
Meeting of the Executive Steering Group on Shortages and Safety of Medicinal Products (MSSG) – September 2025, Online, European Medicines Agency, Amsterdam, the Netherlands, from 24 September 2025, 10:00 (CEST) to 24 September 2025, 12:00 (CEST)
Meeting of the Executive Steering Group on Shortages and Safety of Medicinal Products (MSSG) – April 2025, Online, European Medicines Agency, Amsterdam, the Netherlands, from 29 April 2025, 10:00 (CEST) to 29 April 2025, 12:00 (CEST)