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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

Overview of timetables
modified 13/01/2026

Member: María Teresa Sanz PortilloAlternate: Elisa SulleiroAgencia Española del…
modified 13/01/2026

IMPLEMENTATION OF THE VARIATIONS FRAMEWORK Marketing authorisation holders…
modified 12/01/2026

Added in January 2026 08 January CORRECTION - CMDh Recommendation for…
modified 08/01/2026

CMDh Recommendation for classification of unforeseen variations according to…
modified 08/01/2026

Mock-ups, Specimens and Samples for new applications
modified 07/01/2026

Guidance on the work sharing procedure for the assessment of Active Substance…
modified 07/01/2026

Member: vacant Alternate: Rui Pedro da Costa Vilar INFARMEDParque de Saúde de…
modified 19/12/2025

Marta Marcelino INFARMEDParque de Saúde de LisboaAvenida do Brasil, n°…
modified 19/12/2025

List of active substances for which data has been submitted in accordance with…
modified 18/12/2025

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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