首页 >
法规速递
-
国家药监局药审中心关于发布《基于动物法则的药物研究技术指导原则(试行)》的通告(2023年第26号)-2023/4/7
2023-04-10查看详情 > -
关于公开征求《化学仿制药生物等效性研究摘要(征求意见稿)》意见的通知-2023/10/07
2023-10-08查看详情 > -
Document: EudraVigilance human - Sponsor registration form-2025/1/7
2025-01-08查看详情 > -
Page: Overview of the current regulatory testing requirements for medicinal products for human use and opportunities for implementation of the 3Rs - Scientific guideline-2025/2/13
2025-02-14查看详情 > -
Page: Paediatric investigation plans: questions and answers-2025/3/24
2025-03-25查看详情 > -
Document: FertiPro N.V. HSA-containing ART media - Procedural steps and scientific information after initial consultation (archive)-2025/4/24
2025-04-27查看详情 > -
M13B Bioequivalence for Immediate-Release Solid Oral Dosage Forms: Additional Strengths Biowaiver Draft -2025/5/30
2025-06-06查看详情 > -
Document: 2024 AI Observatory report-2025/7/10
2025-07-11查看详情 > -
关于公开征求《药物临床试验利益相关性声明(试行)(征求意见稿)》意见的通知-2025/8/20
2025-08-21查看详情 > -
Page: Patients' and Consumers' Working Party-2025/9/29
2025-09-30查看详情 >