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Document: European Medicines Agency post-authorisation procedural advice for users of the centralised procedure: document with track changes-2025/7/15
2025-07-16查看详情 > -
Page: Assessment templates and guidance-2025/8/26
2025-08-27查看详情 > -
Document: Products Management Services (PMS) - Implementation of International Organization for Standardization (ISO) standards for the identification of medicinal products (IDMP) in Europe - Chapter 1: Registration requirements-2025/10/2
2025-10-08查看详情 > -
Document: Agenda of the CHMP meeting 10-13 November 2025-2025/11/10
2025-11-11查看详情 > -
Document: Medicine shortage communication (MSC): Insulin lispro Sanofi (insulin lispro 100 units/ml solution for injection in cartridge and pre-filled pen)-2025/12/8
2025-12-09查看详情 > -
中药保护品种公告（第34号）（2026年第11号）-2026/1/20
2026-01-21查看详情 > -
Page: ICH Q2(R2) Validation of analytical procedures - Scientific guideline-2026/2/20
2026-02-27查看详情 > -
Page: Eltrombopag product-specific bioequivalence guidance-2026/3/25
2026-03-26查看详情 > -
Document: Meeting summary - Medicine Shortages SPOC Working Party meeting 16-17 March 2026-2026/5/4
2026-05-06查看详情 > -
Multiple Endpoints in Clinical Trials Guidance for Industry (Final)-2022/10/21
2022-11-15查看详情 >
