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Document: European Medicines Agency post-authorisation procedural advice for users of the centralised procedure: document with tracked changes-2026/1/15
2026-01-16查看详情 > -
Document: Guiding principles of good AI practice in drug development-2026/1/14
2026-01-15查看详情 > -
Page: International Coalition of Medicines Regulatory Authorities (ICMRA)-2026/1/14
2026-01-15查看详情 > -
Document: List of clinical evaluation consultation procedure (CECP) opinions issued for medical devices awaiting finalisation of conformity assessment-2026/1/14
2026-01-15查看详情 > -
Document: Dates of 2026 Scientific Advice Working Party - Human (SAWP-H) meetings and submission deadlines for scientific advice, protocol assistance, qualification of novel methodologies and HTACG/EMA parallel Joint Scientific Consultation (JSC) requests
2026-01-14查看详情 > -
Document: Article 57 product data-2026/1/13
2026-01-14查看详情 > -
Document: Agenda of the CVMP meeting 13-15 January 2026-2026/1/12
2026-01-13查看详情 > -
Document: Agenda of the PRAC meeting 12 - 15 January 2026-2026/1/12
2026-01-13查看详情 > -
Page: Medical devices-2026/1/12
2026-01-13查看详情 > -
Page: Substance and product data management services-2026/1/12
2026-01-13查看详情 >
