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Page: Variations not requiring assessment (veterinary medicines)-2026/3/5
2026-03-06查看详情 > -
Page: Transferring a veterinary marketing authorisation-2026/3/5
2026-03-06查看详情 > -
Page: Pre-authorisation guidance under the Veterinary Medicinal Products Regulation (Regulation (EU) 2019/6)-2026/3/5
2026-03-06查看详情 > -
Page: Clinical trials in human medicines-2026/3/5
2026-03-06查看详情 > -
Document: Agenda - Ad hoc Executive Steering Group on Shortages and Safety of Medicinal Products (MSSG) - 5 March 2026-2026/3/5
2026-03-06查看详情 > -
Page: Plasma master file certificates-2026/3/4
2026-03-05查看详情 > -
Document: List of European Union reference dates (EURD) and frequency of submission of periodic safety update reports (PSURs)-2026/3/4
2026-03-05查看详情 > -
Document: Draft guidance on the conduct of clinical trials during public health emergencies-2026/3/4
2026-03-05查看详情 > -
Document: Records of data processing activity for the handling the contribution towards commuting costs-2026/3/4
2026-03-05查看详情 > -
Page: Data Analysis and Real World Interrogation Network (DARWIN EU)-2026/3/4
2026-03-05查看详情 >
