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Document: Presentation - Emerging and innovative therapies - state of play and key questions (O. Vedin)-2026/8/14

Dosage and Administration Section of Labeling for Human Prescription Drug and Biological Products — Content and Format(Draft)-2023/01/12

Regulatory and procedural guideline: Compilation of Union procedures on inspections and exchange of information-2023/7/13

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Document: Draft reflection paper on the qualification of non-mutagenic impurities-2025/1/30

Document: Minutes of the CHMP meeting on 14-17 October 2024-2025/3/7

Document: List of medicines currently in PRIME scheme-2025/4/9

Document: Orientation guide for delegates - EMA building-2025/5/22

Document: List of changes to combined Veterinary Dictionary for Drug Regulatory Activities (VeDDRA) list of clinical terms for reporting suspected adverse events in animal and humans to veterinary medicinal products for 2024-2025/6/27