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Document: Contact details of national competent authorities for requests of translation exemptions falling under Art. 63.3 of Directive 2001/83/EC and cases of shortages-2025/1/7
2025-01-08查看详情 > -
Page: Budesonide, gastro-resistant hard capsules with prolonged release properties, 3 mg, product-specific bioequivalence guidance-2025/2/12
2025-02-13查看详情 > -
Document: Mandate, objectives and rules of procedure for the CVMP Pharmacovigilance Working Party (PhVWP-V)-2025/3/21
2025-03-24查看详情 > -
Page: Policies and procedures-2025/4/22
2025-04-23查看详情 > -
Document: Minutes of the PRAC meeting 07-10 April 2025-2025/6/4
2025-06-05查看详情 > -
Document: Annex I questions and answers – Fees, charges and remuneration for assessment procedures and services relating to medicinal products for human use-2025/7/10
2025-07-11查看详情 > -
Page: Veterinary Medicines-2025/8/18
2025-08-19查看详情 > -
关于公开征求《药物上市申请临床评价技术指导原则（征求意见稿）》意见的通知-2025/9/29
2025-09-30查看详情 > -
Document: Applications for new human medicines under evaluation: November 2025-2025/11/5
2025-11-06查看详情 > -
Page: Antiviral medicines for pandemic influenza-2025/12/4
2025-12-05查看详情 >
