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Page: PRIME: priority medicines-2025/4/9
2025-04-11查看详情 > -
Document: Orientation guide for patient representatives and healthcare professionals - EMA building-2025/5/22
2025-05-23查看详情 > -
Document: Non-current Veterinary Dictionary for Drug Regulatory Activities (VeDDRA) low level terms (LLT) and codes-2025/6/27
2025-06-30查看详情 > -
Page: Zonisamide product-specific bioequivalence guidance-2025/7/30
2025-07-31查看详情 > -
Document: Quick guide to competing interests for EMA experts-2025/9/17
2025-09-18查看详情 > -
Expanded Access to Investigational Drugs for Treatment Use: Questions and Answers-2025/10/22
2025-10-24查看详情 > -
Document: European Medicines Agency post-authorisation procedural advice for users of the centralised procedure: document with tracked changes-2025/11/26
2025-11-27查看详情 > -
Document: Call for user acceptance testers for the read functionality in the Public Product Management Service (PMS) Application Programming Interface (API)-2025/12/17
2025-12-18查看详情 > -
Document: CHMP work plan 2026-2026/2/3
2026-02-04查看详情 > -
Document: Minutes of the PRAC meeting 12 - 15 January 2026-2026/3/11
2026-03-12查看详情 >