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Document: Key information section in package leaflet of centrally authorised medicinal products: Public consultation-2025/4/14
2025-04-15查看详情 > -
Document: Overview of (invented) names reviewed in April 2025 by the Name Review Group (NRG) adopted at the CHMP meeting of 22 May 2025-2025/5/27
2025-05-28查看详情 > -
Page: Paracetamol product-specific bioequivalence guidance-2025/6/30
2025-07-01查看详情 > -
Page: Recommendations on medication errors-2025/8/1
2025-08-04查看详情 > -
Malaria: Developing Drugs for Treatment-2025/9/23
2025-09-23查看详情 > -
Document: Agenda - ACT EU multi-stakeholder platform annual meeting - October 2025-2025/10/28
2025-10-29查看详情 > -
Document: List of centrally authorised products with safety-related changes to the product information-2025/11/28
2025-12-01查看详情 > -
国家药监局综合司公开征求《化妆品新原料注册备案资料管理规定（修订草案征求意见稿）》意见-2025/12/26
2025-12-29查看详情 > -
Document: Agenda - Webinar on the use of platform technologies in the non-clinical and clinical domains-2026/2/6
2026-02-09查看详情 > -
Document: Release notes - production release version 1.7.2615 March 2026 - Veterinary Medicinal Products Regulation: Union Product Database-2026/3/16
2026-03-17查看详情 >
