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Document: Quality control of medicinal product data submitted as per the legal requirement introduced by Article 57(2) of Regulation (EC) No. 726/2004-2025/6/10
2025-06-11查看详情 > -
Page: Changing the labelling and package leaflet (Article 61(3) notifications)-2025/7/15
2025-07-16查看详情 > -
关于公开征求ICH《E6（R3）：药物临床试验质量管理规范技术指导原则（GCP）》原则及附件1实施建议意见的通知-2025/8/28
2025-08-29查看详情 > -
Page: Fees for human medicines-2025/10/2
2025-10-08查看详情 > -
Document: Agenda - PDCO agenda of the 11-14 November 2025 meeting-2025/11/11
2025-11-12查看详情 > -
Page: Development and manufacture of synthetic peptides - Scientific guideline-2025/12/9
2025-12-10查看详情 > -
Document: Standard operating procedure for procedure to be followed when the incident management plan for medicines for veterinary use is triggered-2026/1/20
2026-01-21查看详情 > -
Page: ICH M4Q - The Common Technical Document for the registration of pharmaceuticals for human use - Quality - Scientific guideline-2026/2/20
2026-02-27查看详情 > -
Page: Clinical Trials Information System (CTIS): training and support-2026/3/26
2026-03-27查看详情 > -
Document: Minutes of the CAT meeting 18-20 March 2026-2026/5/5
2026-05-06查看详情 >
