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Human Medicines

This area of the website provides information relating to the regulation of human medicines, including access to product information, pharmacovigilance and the directory of relevant agencies.

HUMAN MEDICINES | RECENTLY PUBLISHED

RELATED DOCUMENTS EMA has issued guidance documents aligned with the revised…
modified 03/02/2026

Added in February 2026 03 February NEW - 09-11 December CMDh minutes Added in…
modified 03/02/2026

Meeting 9-11 December 2025: Agenda  - MinutesMeeting 11-13 November 2025: Agenda…
modified 03/02/2026

LEGAL FRAMEWORK Regulation (EU) 2024/1701 of 11 March 2024 amending Regulation…
modified 03/02/2026

Contact Points
modified 27/01/2026

Meeting 27-29 January 2026: Agenda
modified 26/01/2026

CMDH AGENDAS AND MINUTES 2026
added 26/01/2026

Template Recommendation form - Article 5 (September 2010)
modified 20/01/2026

National recommendations for requests to act as RMS  (January 2026)
modified 19/01/2026

IMPLEMENTATION OF THE VARIATIONS FRAMEWORK Marketing authorisation holders…
modified 19/01/2026

For the United Kingdom, as of 1 January 2021, European Union law applies only to the territory of Northern Ireland (NI) to the extent foreseen in the Protocol on Ireland / NI.

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