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Document: Quality Review of Documents (QRD) annotated template v11: Draft for public consultation - track changes-2025/4/14
2025-04-15查看详情 > -
Document: Minutes of the CHMP meeting 9-12 December 2024-2025/5/27
2025-05-28查看详情 > -
Page: Prasugrel product-specific bioequivalence guidance-2025/6/30
2025-07-01查看详情 > -
Document: Organisation chart: Information Management-2025/8/1
2025-08-04查看详情 > -
Consideration of Enforcement Policies for In Vitro Diagnostic Tests During a Section 564 Declared Emergency-2025/9/23
2025-09-23查看详情 > -
Document: Article 57 product data-2025/10/28
2025-10-29查看详情 > -
Page: Plasma master file certificates-2025/11/28
2025-12-01查看详情 > -
10句话讲清药械妆“两个档案”-2025/12/26
2025-12-29查看详情 > -
Page: Drug Shortages Global Regulatory Working Group-2026/2/6
2026-02-09查看详情 > -
Page: Procedures for monograph and list entry establishment-2026/3/16
2026-03-17查看详情 >
