首页 >
法规速递
-
Document: Questions and answers on implementation of the medical devices and in vitro diagnostic medical devices Regulations ((EU) 2017/745 and (EU) 2017/746) - tracked changes-2025/2/5
2025-02-10查看详情 > -
Document: Questions and answers on implementation of the medical devices and in vitro diagnostic medical devices Regulations ((EU) 2017/745 and (EU) 2017/746)-2025/2/5
2025-02-10查看详情 > -
Document: List of European Union reference dates (EURD) and frequency of submission of periodic safety update reports (PSURs)-2025/2/5
2025-02-06查看详情 > -
Page: Executive Steering Group on Shortages and Safety of Medicinal Products (MSSG) meetings-2025/2/5
2025-02-06查看详情 > -
Page: Clinical Trials Information System (CTIS): training and support-2025/2/5
2025-02-06查看详情 > -
Document: Appendix 1: Acceptable intakes established for N-nitrosamines-2025/2/5
2025-02-06查看详情 > -
Page: Vaccines Working Party-2025/2/4
2025-02-05查看详情 > -
Page: Methodology Working Party-2025/2/4
2025-02-05查看详情 > -
Page: 3Rs Working Party-2025/2/4
2025-02-05查看详情 > -
Page: Quality Working Party-2025/2/4
2025-02-05查看详情 >
