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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

Vaqta (hepatitis A vaccine) End of procedure: 19/12/2013 Date of…
modified 07/08/2026

Verorab (rabies virus, inactivated)FR/W/0028/pdWS/001End of procedure:…
modified 07/08/2026

Valtrex (valaciclovir) End of procedure: 09/12/2019 Date of publication:…
modified 07/08/2026

Added in August 2026 04 August UPDATE - Guidance published by Member States on…
modified 04/08/2026

Guidance published by Member States on the implementation of the Falsified…
modified 04/08/2026

CMDh letter for MAHs for medicinal products containing active ingredients in the…
added 04/08/2026

CMDh Multi-Annual Workplan to 2020 (April 2016)
modified 03/08/2026

EMA/CMDh explanatory notes on Variation Application Form - Human medicinal…
modified 30/07/2026

Templates Variation Assessment Report
modified 30/07/2026

Best Practice Guides (BPGs) for the Submission and Processing of Variations in…
modified 30/07/2026

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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