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Document: Checklist for annual updates for parallel distribution: guidance for industry-2025/1/6
2025-01-07查看详情 > -
Document: Applications for new human medicines under evaluation: February 2025-2025/2/10
2025-02-11查看详情 > -
Page: ICH M11 guideline, clinical study protocol template and technical specifications - Scientific guideline-2025/3/18
2025-03-19查看详情 > -
Document: Business process description for expert management-2025/4/22
2025-04-23查看详情 > -
Page: Plasma master file certificates-2025/6/2
2025-06-03查看详情 > -
Document: CHMP PROM minutes for the meeting on 20 January 2025-2025/7/8
2025-07-09查看详情 > -
Document: Product Management Services (PMS) - Implementation of International Organization for Standardization (ISO) standards for the identification of medicinal products (IDMP) in Europe - Chapter 2 - track changes-2025/8/8
2025-08-10查看详情 > -
Page: Innovation Task Force briefing meetings-2025/9/25
2025-09-26查看详情 > -
Document: Agenda - 1st EMA and European Respiratory Society (ERS) bilateral meeting-2025/11/4
2025-11-05查看详情 > -
Page: EudraVigilance: electronic reporting-2025/12/3
2025-12-04查看详情 >
