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Page: European Sales and Use of Antimicrobials for Veterinary Medicine (ESUAvet) annual surveillance reports-2025/12/9
2025-12-10查看详情 > -
M4Q(R2) The Common Technical Document for the Registration of Pharmaceuticals for Human Use: Quality-2026/1/20
2026-01-21查看详情 > -
Page: ICH E22 General considerations for patient preference studies - Scientific guideline-2026/2/24
2026-02-27查看详情 > -
Document: Template - Application for transfer of marketing authorisation from transferor to transferee - cover letter (human)-2026/3/27
2026-03-30查看详情 > -
国家药品监督管理局 公安部 国家卫生健康委员会 国家市场监督管理总局 国家医疗保障局 国家中医药管理局 国家疾病预防控制局关于发布《医药代表管理办法》的公告(2026年第42号)-2026/5/7
2026-05-08查看详情 > -
Submitting Clinical Trial Datasets to Evaluate the Impact of Immunogenicity on the Pharmacokinetics of a Drug -2026/6/18
2026-06-21查看详情 > -
Bioanalytical method validation-2022/10/25
2022-11-15查看详情 > -
国家药监局关于修订注射用人白介素-11说明书的公告(2023年第58号)-2023/4/25
2023-04-25查看详情 > -
关于《药物临床试验样本量估计指导原则(征求意见稿)》公开征求意见的通知-2023/10/30
2023-11-06查看详情 > -
Document: Policy 58: European Medicines Agency policy on the handling of competing interests of Management Board members - effective from May 2025-2025/1/14
2025-01-15查看详情 >