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Document: European Shortages Monitoring Platform (ESMP): Marketing authorisation holder reporting templates-2025/5/13
2025-05-14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-2025/6/19
2025-06-20查看详情 > -
Document: Innovation Task Force (ITF) briefing meeting report-2025/7/24
2025-07-25查看详情 > -
Document: Medicinal products for human use: monthly figures - August 2025-2025/9/9
2025-09-10查看详情 > -
Document: Timetable: Post-authorisation measure (PAM) assessed by PRAC-2025/10/14
2025-10-15查看详情 > -
Document: Scientific advice and protocol assistance adopted during the CHMP meeting 13-16 October 2025-2025/11/18
2025-11-19查看详情 > -
Document: Guideline on the clinical investigation of medicinal products in the treatment of patients with acute respiratory distress syndrome - Revision 2-2025/12/12
2025-12-15查看详情 > -
Page: Clinical investigation of medicinal products in the treatment of peripheral-arterial occlusive disease - Scientific guideline-2026/1/27
2026-01-28查看详情 > -
New Clinical Investigation Exclusivity (3-Year Exclusivity) for Drug Products: Questions and Answers-2026/3/3
2026-03-05查看详情 > -
Page: Core summary of product characteristics for human normal immunoglobulin for subcutaneous and intramuscular use - Scientific guideline-2026/4/1
2026-04-02查看详情 >