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Document: Annex to 24-27 February 2025 CHMP Agenda-2025/2/24
2025-02-25查看详情 > -
Document: Organisation chart: Veterinary Medicines-2025/4/1
2025-04-02查看详情 > -
国家药监局关于批准注册266个医疗器械产品的公告(2025年4月)(2025年第48号)-2025/5/13
2025-05-14查看详情 > -
Document: Code of conduct of the European Medicines Agency-2025/6/19
2025-06-20查看详情 > -
Document: Guideline on good pharmacovigilance practices (GVP) - Module VI Addendum II – Masking of personal data in individual case safety reports submitted to EudraVigilance-2025/7/24
2025-07-25查看详情 > -
Page: Supporting innovation-2025/9/9
2025-09-10查看详情 > -
Document: Suvaxyn Circo+MH RTU : EPAR - Public assessment report-2025/10/14
2025-10-15查看详情 > -
Document: Dates of 2025 Scientific Advice Working Party - Human (SAWP-H) meetings and submission deadlines for scientific advice, protocol assistance, qualification of novel methodologies and HTACG/EMA parallel Joint Scientific Consultation (JSC) requests
2025-11-19查看详情 > -
Document: Union list of critical medicines-2025/12/12
2025-12-15查看详情 > -
织密药品安全法治网 促进药品高水平安全和医药产业高质量发展-2026/1/27
2026-01-28查看详情 >
