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Document: Quality Review of Documents (QRD) annotated template v11: From for submission of comments to public consultation-2025/4/14
2025-04-15查看详情 > -
Document: Start of procedure - extension of marketing authorisation (26 April - 22 May 2025)-2025/5/27
2025-05-28查看详情 > -
Page: Guidance on the application of the revised variations framework-2025/6/30
2025-07-01查看详情 > -
CVM GFI #294 - Animal Food Ingredient Consultation (AFIC)-2025/7/31
2025-08-04查看详情 > -
Document: MedDRA important medical event terms list - version 28.1-2025/9/23
2025-09-24查看详情 > -
Page: Plasma master file certificates-2025/10/28
2025-10-29查看详情 > -
Document: Guidance for stepwise PIPs (sPIPs)-2025/11/28
2025-12-01查看详情 > -
国家药监局药审中心关于发布《治疗慢性气道疾病的靶向炎症因子类生物制剂临床试验技术指导原则（试行）》的通告（2025年第51号）-2025/12/30
2025-12-31查看详情 > -
Document: Overview of (invented) names reviewed in November 2025 by the Name Review Group (NRG) adopted at the CHMP meeting of 11 December 2025-2026/2/6
2026-02-09查看详情 > -
Page: Stakeholders and Communication-2026/3/16
2026-03-17查看详情 >
