Quick Response (QR) codes in the labelling and/or package leaflet of veterinary medicinal products authorised via the centralised (CP), mutual recognition (MRP), decentralised procedures (DCP) and national procedures

Webinar on the Union Product Database Data Quality Framework, Online, European Medicines Agency, Amsterdam, the Netherlands, from 11 January 2024, 15:00 (CET) to 11 January 2024, 16:30 (CET)

EVVet3 EVWeb Production – Release notes

EVVET - EVWEB user manual

HMPC: overview of assessment work - priority list

Committee for Medicinal Products for Human Use (CHMP): 11-14 December 2023, European Medicines Agency, Amsterdam, the Netherlands, from 11 December 2023 to 14 December 2023

Agenda of the CHMP meeting 11-14 December 2023

Procedures for monograph and list entry establishment

Expected publication dates of PRAC recommendations on safety signals

Human medicines European public assessment report (EPAR): Truxima, rituximab, Date of authorisation: 17/02/2017, Revision: 21, Status: Authorised