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Document: Overview of comments received on Q&A regarding co-processed excipients used in solid oral dosage forms H and V (EMA/CHMP/CVMP/QWP/422493/2024)-2026/2/16
2026-02-26查看详情 > -
《药品现代物流规范化建设指导意见》政策问答-2026/3/25
2026-03-26查看详情 > -
Document: Annexes to ICH Q3C guideline on impurities: guideline for residual solvents (EMA/CHMP/ICH/82260/2006) and VICH GL18 Impurities: residual solvents in new veterinary medicinal products, active substances and excipients (EMA/CVMP/VICH/502/1999) - R
2026-04-30查看详情 > -
Size, Shape, and Other Physical Attributes of Generic Tablets and Capsules (Final)-2022/10/3
2022-11-14查看详情 > -
国家药监局药审中心关于发布《成人用药数据外推至儿科人群的定量方法学指导原则（试行）》的通告（2023年第27号）-2023/4/12
2023-04-13查看详情 > -
国家药监局 国家卫生健康委关于发布实施《中华人民共和国药典》（2020年版）第一增补本的公告（2023年第126号）-2023/10/12
2023-10-13查看详情 > -
Document: New product information wording – Extracts from PRAC recommendations on signals adopted at the 25-28 November 2024 PRAC-2025/1/7
2025-01-08查看详情 > -
Page: EU Innovation Network (EU-IN)-2025/2/13
2025-02-14查看详情 > -
Document: Minutes of the CVMP meeting 11-12 February 2025-2025/3/25
2025-03-26查看详情 > -
国家药监局关于中药保护品种的公告(延长保护期第22号)(2025年第44号)-2025/4/28
2025-04-29查看详情 >
