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Document: Timetable: Annual renewal application of conditional marketing authorisation - ATMP-2026/5/27
2026-05-28查看详情 > -
Document: Minutes - Enpr-EMA Coordinating Group meeting, April 2026-2026/7/10
2026-07-11查看详情 > -
Document: Presentation - Challenges and opportunities in medicines development (A. Baczynska)-2026/8/14
2026-08-17查看详情 > -
Format and Content of a REMS Document Guidance for Industry(Final)-2023/01/04
2023-01-04查看详情 > -
Guidance on good manufacturing practice and good distribution practice: Questions and answers-2023/7/13
2023-07-21查看详情 > -
Page: ICH Q14 Analytical procedure development - Scientific guideline-2024/1/26
2024-03-11查看详情 > -
Document: Procedural advice for post-orphan medicinal product designation activities: Guidance for sponsors-2025/1/30
2025-02-05查看详情 > -
Page: COVID-19 medicines-2025/3/7
2025-03-10查看详情 > -
Document: Amended Biologics Working Party Vaccines Quality Operational Expert Group (BV-OEG) Influenza Meeting: EU recommendations for the seasonal influenza vaccine composition for the season 2025/2026-2025/4/9
2025-04-11查看详情 > -
Document: Agenda - EMA’s 30th anniversary scientific conference-2025/5/22
2025-05-23查看详情 >
