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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 > -
Document: Draft user manual for the eXtended EudraVigilance Medicinal Product Dictionary (XEVMPD) user interface (XEVMPDweb)-2025/12/10
2025-12-11查看详情 > -
Document: Scientific advice and protocol assistance adopted during the CHMP meeting 8-11 December 2025-2026/1/23
2026-01-26查看详情 > -
Page: Quality of medicines: questions and answers - Part 1-2026/3/2
2026-03-03查看详情 > -
Document: EU implementation strategy of ICH E2D(R1) Guideline - Post-approval safety data: Definitions and standards for management and reporting of individual case safety reports-2026/3/27
2026-03-30查看详情 > -
Document: Applications for new human medicines under evaluation: May 2026-2026/5/11
2026-05-12查看详情 > -
Page: Cookies-2026/6/24
2026-06-25查看详情 >