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Document: Article 57 product data-2026/3/19
2026-03-20查看详情 > -
Document: IRIS guide for applicants - How to create, submit and manage IRIS applications, for industry and individual applicants-2026/3/19
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Document: QRD veterinary Appendix I - Adverse event (PhV) MSs reporting details-2026/3/19
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Document: Innovation Task Force (ITF) briefing meeting request form-2026/3/19
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Document: 2025 Annual Report on EudraVigilance for the European Parliament, the Council and the Commission-2026/3/19
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Document: Timetable: Safety signal - Assessment of responses to request for supplementary information (RSI) - ATMP-2026/3/19
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Document: Timetable: Safety signal - Assessment of responses to request for supplementary information (RSI)-2026/3/19
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Document: EU Implementation Guide (IG) on veterinary medicines product data in the Union Product Database - Chapter 5: Technical specifications-2026/3/19
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Document: List of withdrawn medicinal products in accordance with Art. 123(4) of the Directive (1 January - 31 December 2025)-2026/3/19
2026-03-20查看详情 > -
Page: PRIME: priority medicines-2026/3/18
2026-03-19查看详情 >