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法规速递
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Draft Guidance: Decentralized Clinical Trials for Drugs, Biological Products, and Devices-2023/5/2
2023-05-04查看详情 > -
Final Guidance: Submitting Clinical Trial Datasets and Documentation for Clinical Outcome Assessments Using Item Response Theory-2023/11/3
2023-11-07查看详情 > -
Page: Pre-authorisation guidance under the Veterinary Medicinal Products Regulation (Regulation (EU) 2019/6)-2025/1/15
2025-01-16查看详情 > -
Document: Minutes - DARWIN EU Advisory Board - 3 May 2024-2025-2025/2/20
2025-02-21查看详情 > -
Document: Policy 85: Identity and Access Management to EMA IT Systems-2025/3/28
2025-04-01查看详情 > -
Document: List of signals discussed at PRAC since September 2012-2025/5/5
2025-05-06查看详情 > -
Page: Administration and Corporate Management-2025/6/16
2025-06-17查看详情 > -
Page: Regulatory science research needs-2025/7/18
2025-07-21查看详情 > -
Document: Appendix 1: Acceptable intakes established for N-nitrosamines-2025/9/2
2025-09-03查看详情 > -
Document: Q&A on impact of EU-USA Mutual Recognition Agreement on marketing authorisation applications and relevant variations - Revised 1st October 2025-2025/10/7
2025-10-08查看详情 >
