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Document: Member states contact points for translations review-2026/3/25
2026-03-26查看详情 > -
Page: Tafamidis soft gelatin capsules 20 mg and 61 mg product-specific bioequivalence guidance-2026/4/30
2026-05-02查看详情 > -
Competitive Generic Therapies (Final)-2022/10/5
2022-11-15查看详情 > -
关于公开征求《药品监管信息化标准体系（征求意见稿）》-2023/4/11
2023-04-14查看详情 > -
《药品经营和使用质量监督管理办法》政策解读-2023/10/13
2023-10-13查看详情 > -
Document: IRIS guide for applicants - How to create and submit scientific applications, for industry and individual applicants-2025/1/8
2025-01-09查看详情 > -
Page: Guideline on assessment and reporting of mechanistic models used in the context of model informed drug development-2025/2/14
2025-02-18查看详情 > -
Document: European Medicines Agency post-authorisation procedural advice for users of the centralised procedure: document with track changes-2025/3/25
2025-03-26查看详情 > -
Page: Vaccine-preventable diseases: key facts-2025/4/28
2025-04-29查看详情 > -
Document: QRD veterinary product-information template version 9.1-2025/6/5
2025-06-06查看详情 >
