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Document: Minutes of the CHMP meeting 11-14 November 2024-2025/3/7
2025-03-10查看详情 > -
Page: Website outages and upgrades-2025/3/7
2025-03-10查看详情 > -
Document: List of withdrawn medicinal products in accordance with Art. 123(4) of the Directive (1 January - 31 December 2024)-2025/3/7
2025-03-10查看详情 > -
Document: List of European Union reference dates (EURD) and frequency of submission of periodic safety update reports (PSURs)-2025/3/5
2025-03-06查看详情 > -
Document: Annex to 24-27 February 2025 CHMP Agenda-2025/3/5
2025-03-06查看详情 > -
Document: Frequently asked questions (FAQs) : How to create and submit an annual safety report and respond to related requests for information - CTIS Training Programme - Module 18-2025/3/5
2025-03-06查看详情 > -
Document: Frequently asked questions (FAQs): How to create, submit and withdraw a Clinical Trial Application - CTIS Training Programme - Module 10-2025/3/5
2025-03-06查看详情 > -
Document: Minutes - PDCO minutes of the 12-15 November 2024 meeting-2025/3/5
2025-03-06查看详情 > -
Page: CHMP opinions on consultation procedures-2025/3/5
2025-03-06查看详情 > -
Document: Vitrolife IVF media - Procedural steps and scientific information after initial consultation-2025/3/5
2025-03-06查看详情 >