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Document: Infographic - Orphan Medicines in the EU-2025/2/27
2025-03-03查看详情 > -
Document: Guidance on the details of the classification of variations requiring assessment according to Article 62 of Regulation (EU) 2019/6 for veterinary medicinal products and on the documentation to be submitted pursuant to those variations-2025/2/27
2025-03-03查看详情 > -
Document: Clinical Trial Information System (CTIS) evaluation timelines-2025/2/27
2025-03-03查看详情 > -
Document: Annex - National provisions for SMEs applicable to the pharmaceutical sector-2025/2/26
2025-02-27查看详情 > -
Document: Agenda - EMA Veterinary Innovation Day - March 2025-2025/2/26
2025-02-27查看详情 > -
Page: ICH Guideline M13A on bioequivalence for immediate-release solid oral dosage forms - Scientific guideline-2025/2/26
2025-02-27查看详情 > -
Page: Investigation of bioequivalence - Scientific guideline-2025/2/26
2025-02-27查看详情 > -
Page: Website outages and upgrades-2025/2/26
2025-02-27查看详情 > -
Page: Website outages and upgrades-2025/2/26
2025-02-27查看详情 > -
Document: Agenda - PDCO agenda of the 25-28 February 2025 meeting-2025/2/26
2025-02-27查看详情 >
