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关于公开征求《化学药品批准后药学变更管理方案技术指导原则（征求意见稿）》意见的通知-2025/6/9
2025-06-10查看详情 > -
Document: Template - Application for transfer of marketing authorisation from transferor to transferee - cover letter (human)-2025/7/15
2025-07-16查看详情 > -
Page: Clinical Trials Regulation: progress on implementation-2025/8/26
2025-08-27查看详情 > -
Document: Organisation chart: Advisory functions-2025/10/1
2025-10-08查看详情 > -
图解海报 | 《医疗器械生产质量管理规范》系列解读（一）-2025/11/10
2025-11-11查看详情 > -
Document: Medicinal products for human use: monthly figures - November 2025-2025/12/8
2025-12-09查看详情 > -
Document: Deadlines for submission of applications for orphan medicinal product designation to the EMA and corresponding COMP timetable for valid applications 2026-2027-2026/1/19
2026-01-20查看详情 > -
Page: Risk management requirements for elemental impurities in veterinary medicinal products - Scientific guideline-2026/2/20
2026-02-27查看详情 > -
Document: QRD Appendix V - Adverse-drug-reaction reporting details-2026/3/25
2026-03-26查看详情 > -
Document: List of eligible industry stakeholder organisations-2026/5/4
2026-05-06查看详情 >
