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Document: 2024 European Medicines Agency annual report on independence-2025/3/19
2025-03-20查看详情 > -
Page: Applying for marketing authorisation: orphan medicines-2025/3/19
2025-03-20查看详情 > -
Document: Clinical Trial Information System (CTIS) structured data form - Initial application, additional Member State Concerned, substantial modification, non-substantial modification-2025/3/18
2025-03-19查看详情 > -
Page: Variations requiring assessment (veterinary medicines)-2025/3/18
2025-03-19查看详情 > -
Document: Agenda of the CAT meeting 19-21 March 2025-2025/3/18
2025-03-19查看详情 > -
Page: ICH M11 guideline, clinical study protocol template and technical specifications - Scientific guideline-2025/3/18
2025-03-19查看详情 > -
Document: ICH M11 Technical Specification - Updated step 2b-2025/3/18
2025-03-19查看详情 > -
Page: CVMP recommendations on limited market classification and eligibility for authorisation under Article 23-2025/3/18
2025-03-19查看详情 > -
Document: Seizing opportunities in a changing medicines landscape: The European medicines agencies network strategy 2028 (final)-2025/3/18
2025-03-19查看详情 > -
Document: Analysis and summaries of public consultation results: The European medicines agencies network strategy to 2028-2025/3/18
2025-03-19查看详情 >
