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国家药监局综合司公开征求《关于优化全生命周期监管 支持高端医疗器械创新发展的举措(征求意见稿)》意见-2025/3/31
2025-04-01查看详情 > -
Document: PRAC recommendations on signals adopted at the 7-10 April 2025 meeting-2025/5/5
2025-05-06查看详情 > -
Document: Release notes - production release version 1.7.2523 - 16 June 2025 - Veterinary Medicinal Products Regulation: Union Product Database-2025/6/16
2025-06-17查看详情 > -
关于公开征求《化学仿制药参比制剂目录(第九十六批)》(征求意见稿)意见的通知-2025/7/18
2025-07-21查看详情 > -
Document: EU Implementation Guide (IG) on veterinary medicines product data in the Union Product Database - Chapter 4: Process and format for the submission of legacy data on veterinary medicinal products (obsolete)-2025/9/2
2025-09-03查看详情 > -
Page: CAT: Working parties and other groups-2025/10/6
2025-10-08查看详情 > -
Document: Concept paper on a paediatric update of the guideline on clinical investigation of medicinal products for the management of Crohn’s disease-2025/11/13
2025-11-14查看详情 > -
Page: List of medicines under additional monitoring-2025/12/10
2025-12-11查看详情 > -
Document: New product information wording: extracts from PRAC recommendations on signals adopted at the 7-10 July 2025 PRAC-2026/1/22
2026-01-23查看详情 > -
Questions and Answers About Requirements for Additional Traceability Records for Certain Foods-2026/2/19
2026-02-27查看详情 >