首页 >
法规速递
-
Page: Non-clinical Working Party-2025/4/15
2025-04-16查看详情 > -
Document: Annex to 27-30 January 2025 CHMP Minutes-2025/5/28
2025-05-29查看详情 > -
Page: Ibuprofen product-specific bioequivalence guidance-2025/7/1
2025-07-02查看详情 > -
关于公开征求《关于开发适宜药品包装规格的指导原则》意见的通知-2025/8/5
2025-08-06查看详情 > -
Document: Timetable: Post-authorisation safety study (PASS) protocols and final results-2025/9/23
2025-09-24查看详情 > -
Document: List of medicinal products under additional monitoring-2025/10/29
2025-10-30查看详情 > -
Page: Pre-authorisation guidance under the Veterinary Medicinal Products Regulation (Regulation (EU) 2019/6)-2025/11/28
2025-12-01查看详情 > -
国家药监局关于修订贝伐珠单抗注射液说明书的公告（2025年第130号） -2025/12/31
2026-01-03查看详情 > -
Page: Fees for veterinary medicines-2026/2/6
2026-02-09查看详情 > -
Physicochemical and Structural (Q3) Characterization of Topical Drug Products Submitted in ANDAs-2026/3/17
2026-03-18查看详情 >
