List of European Union reference dates (EURD) and frequency of submission of periodic safety update reports (PSURs)

Implantable cardiac devices (various) - Notified body 2797 - 15/07/2025 - Expert decision and opinion in the context of the clinical evaluation consultation procedure (CECP)

List of clinical evaluation consultation procedure (CECP) opinions issued for medical devices awaiting finalisation of conformity assessment

Meeting of the Medicine Shortages Single Point of Contact (SPOC) Working Party, Online, from 17 February 2026, 09:30 (CET) to 17 February 2026, 13:00 (CET)

List of centrally authorised products with safety-related changes to the product information

Pharmaceutical industry

Newsletters

Referral: Ipidacrine-containing medicinal products, ipidacrine Article 31 referrals Under evaluation, 30/03/2026

Human medicines European public assessment report (EPAR): Finlee, dabrafenib, Date of authorisation: 15/11/2023, Revision: 9, Status: Authorised

Human medicines European public assessment report (EPAR): Alyftrek, deutivacaftor / tezacaftor / vanzacaftor, Date of authorisation: 30/06/2025, Revision: 3, Status: Authorised