首页 >
法规速递
-
Regulatory and procedural guideline: European Medicines Agency post-authorisation procedural advice for users of the centralised procedure (updated)-2023/11/13
2023-11-15查看详情 > -
Page: Emergency Task Force (ETF)-2025/1/16
2025-01-17查看详情 > -
Page: How to recognise scams using EMA credentials-2025/2/20
2025-02-21查看详情 > -
Page: History of EMA-2025/3/28
2025-04-01查看详情 > -
Document: Minutes - Executive Steering Group on Shortages and Safety of Medicinal Products (MSSG) (April 2025)-2025/5/6
2025-05-07查看详情 > -
Document: Agenda of the CHMP meeting 16-19 June 2025-2025/6/16
2025-06-17查看详情 > -
E21 Inclusion of Pregnant and Breastfeeding Women in Clinical Trials-2025/7/21
2025-07-21查看详情 > -
国家药监局关于注销全自动医用PCR分析仪等2个医疗器械注册证书的公告（2025年第83号）-2025/9/4
2025-09-05查看详情 > -
Document: Agenda - Instrument for Pre-accession Assistance (IPA) training on assessing medicinal products in the EU: A practical introduction-2025/10/7
2025-10-08查看详情 > -
Document: Questions and answers on classification of a product as intended for a limited market according to Article 4(29) and/or eligibility for authorisation according to Article 23 (Applications for limited markets)-2025/11/14
2025-11-17查看详情 >
