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Document: PRAC rapporteur post-authorisation-safety-study-protocol assessment-report template-2026/2/4
2026-02-05查看详情 > -
Document: Template PRAC assessment report of an non-interventional imposed PASS final study report-2026/2/4
2026-02-05查看详情 > -
Page: National competent authorities (human)-2026/2/4
2026-02-05查看详情 > -
Document: List of European Union reference dates (EURD) and frequency of submission of periodic safety update reports (PSURs)-2026/2/4
2026-02-05查看详情 > -
Document: Plasma Master File (PMF) requirements - questions and answers for PMF holders-2026/2/4
2026-02-05查看详情 > -
Document: List of clinical evaluation consultation procedure (CECP) opinions issued for medical devices awaiting finalisation of conformity assessment-2026/2/3
2026-02-04查看详情 > -
Document: Three-year work plan for the Quality Drafting Group (QDG) of the Committee on Herbal Medicinal Products (HMPC)-2026/2/3
2026-02-04查看详情 > -
Document: CHMP work plan 2026-2026/2/3
2026-02-04查看详情 > -
Document: Training module EV-M8 - Considerations on the international transfer of personal (health) data in ICSRs -SUSARs originating in the EU-2026/2/2
2026-02-03查看详情 > -
Page: Pre-authorisation guidance under the Veterinary Medicinal Products Regulation (Regulation (EU) 2019/6)-2026/2/2
2026-02-03查看详情 >