2025 Annual Report on EudraVigilance for the European Parliament, the Council and the Commission

Timetable: Safety signal - Assessment of responses to request for supplementary information (RSI) - ATMP

Timetable: Safety signal - Assessment of responses to request for supplementary information (RSI)

EU Implementation Guide (IG) on veterinary medicines product data in the Union Product Database - Chapter 5: Technical specifications

List of withdrawn medicinal products in accordance with Art. 123(4) of the Directive (1 January - 31 December 2025)

PSUSA/00001324/202505

PSUSA/00001040/202507

PSUSA/00002149/202505

PSUSA/00001672/202508

Human medicines European public assessment report (EPAR): Deltyba, delamanid, Date of authorisation: 27/04/2014, Date of refusal: 25/07/2013, Revision: 28, Status: Authorised