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Page: Quality of medicines questions and answers: Part 2-2025/5/28
2025-05-29查看详情 > -
Page: QRD guidance on the use of adopted abbreviations and pictograms on the packaging of veterinary medicinal products authorised via the centralised (CP), mutual recognition (MRP), decentralised (DCP), subsequent recognition (SRP) and national procedure
2025-07-02查看详情 > -
国家药监局药审中心关于发布《药审中心外聘专家增补名单（2025年第一批、第二批）》的通告（2025年第35号）-2025/8/6
2025-08-06查看详情 > -
Document: Scientific recommendations on classification of advanced therapy medicinal products-2025/9/23
2025-09-24查看详情 > -
Page: Clinical Trials Information System-2025/10/29
2025-10-30查看详情 > -
Page: National competent authorities (human)-2025/11/28
2025-12-01查看详情 > -
国家药监局关于发布仿制药参比制剂目录（第一百批）的通告（2025年第49号） -2025/12/31
2026-01-03查看详情 > -
Page: Good pharmacovigilance practices (GVP)-2026/2/6
2026-02-09查看详情 > -
Document: Agenda - Management Board meeting: 12 March 2026-2026/3/17
2026-03-18查看详情 > -
国家药监局综合司 海关总署办公厅关于印发《允许药材进口口岸现场评估标准及检查细则》的通知-2026/4/20
2026-04-21查看详情 >
