首页 >
法规速递
-
Document: Agenda - Management Board meeting: 11-12 June 2025-2025/6/10
2025-06-11查看详情 > -
Page: Type-IA variations: questions and answers-2025/7/15
2025-07-16查看详情 > -
Document: Highlight report from the 14th Industry stakeholder platform on research and development support-2025/8/27
2025-08-28查看详情 > -
Document: Agenda - HMA/EMA Annual Data Forum 2025-2025/11/10
2025-11-11查看详情 > -
国家药监局关于37批次不符合规定化妆品的通告（2025年第45号）-2025/12/9
2025-12-10查看详情 > -
Document: Questions and answers on signal management-2026/1/20
2026-01-21查看详情 > -
Document: Minutes of the CVMP meeting 2-4 December 2025-2026/2/20
2026-02-27查看详情 > -
Document: Records of data processing activity on processing of personal data pertaining to staff absence-2026/3/25
2026-03-26查看详情 > -
Document: Questions and answers on implementation of Ph.Eur. Medicinal Product Monographs (MPM)-2026/5/5
2026-05-06查看详情 > -
Scientific guideline: Reflection paper on the use of interactive response technologies (interactive voice/web response systems) in clinical trials, with particular emphasis on the handling of expiry dates-2022/10/6
2022-11-15查看详情 >
