首页 >
法规速递
-
Page: Falsified medicines: overview-2025/1/30
2025-02-05查看详情 > -
Document: Minutes of the CHMP meeting 11-14 November 2024-2025/3/7
2025-03-10查看详情 > -
Document: Recommendations on eligibility to PRIME scheme - Adopted at the CHMP meeting of 24-27 March 2025-2025/4/9
2025-04-11查看详情 > -
Document: Orientation guide for industry - EMA building-2025/5/22
2025-05-23查看详情 > -
Document: Combined VeDDRA list of clinical terms for reporting suspected adverse events in animals and humans to veterinary medicinal products-2025/6/27
2025-06-30查看详情 > -
Document: List of European Union reference dates (EURD) and frequency of submission of periodic safety update reports (PSURs)-2025/7/30
2025-07-31查看详情 > -
Page: Website outages and upgrades-2025/9/17
2025-09-18查看详情 > -
Page: Non-human primates in safety testing of human medicinal products and opportunities for 3Rs implementation - Scientific guideline-2025/10/23
2025-10-24查看详情 > -
Page: Vaccines for pandemic influenza-2025/11/25
2025-11-26查看详情 > -
Document: Overview of (invented) names reviewed in November 2025 by the Name Review Group (NRG) adopted at the CHMP meeting of 11 December 2025-2025/12/17
2025-12-18查看详情 >