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FDA Records Access Authority for Cosmetic Products-2026/1/21
2026-01-22查看详情 > -
Page: Fees payable to the European Medicines Agency: Guidance for all applicants-2026/2/25
2026-02-27查看详情 > -
Page: Extensions of marketing authorisations: questions and answers-2026/3/27
2026-03-30查看详情 > -
Clostridioides difficile Infection: Developing Drugs for Treatment, Reduction of Recurrence, and Prevention-2026/5/8
2026-05-09查看详情 > -
Regulatory and procedural guideline: List of centrally authorised products requiring a notification of a change for update of annexes -2023/4/25
2023-04-26查看详情 > -
Draft Guidance: Remote Interactive Evaluations of Drug Manufacturing and Bioresearch Monitoring Facilities-2023/10/25
2023-11-07查看详情 > -
Document: Timetable: Extension application - ATMP-2025/1/14
2025-01-15查看详情 > -
Page: Changing the labelling and package leaflet (Article 61(3) notifications)-2025/2/18
2025-02-19查看详情 > -
Document: Fields and business rules for the European Shortages Monitoring Platform (ESMP) API datasets-2025/3/27
2025-03-28查看详情 > -
Document: Agenda of the HMPC meeting 5-7 May 2025-2025/5/2
2025-05-06查看详情 >
