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Document: List of medicinal products under additional monitoring-2025/11/26
2025-11-27查看详情 > -
Processes and Practices Applicable to Bioresearch Monitoring Inspections-2025/12/19
2025-12-19查看详情 > -
Page: Interested Parties to the HMPC-2026/2/4
2026-02-05查看详情 > -
国家药监局关于批准注册235个医疗器械产品的公告（2026年2月）（2026年第25号）-2026/3/13
2026-03-16查看详情 > -
Page: CHMP opinions on consultation procedures on ancillary substances incorporated in a medical device-2026/4/10
2026-04-12查看详情 > -
Document: 20 years supporting small and medium enterprises (SMEs) at EMA report-2026/5/28
2026-05-29查看详情 > -
Document: European Medicines Agency post-authorisation procedural advice for users of the centralised procedure-2026/7/13
2026-07-14查看详情 > -
Page: International Coalition of Medicines Regulatory Authorities (ICMRA)-2026/8/18
2026-08-19查看详情 > -
Mpox: Development of Drugs and Biological Products; Guidance for Industry(Draft)-2023/01/19
2023-01-19查看详情 > -
Regulatory and procedural guideline: List of centrally authorised products requiring a notification of a change for update of annexes-2023/7/25
2023-07-28查看详情 >
