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Page: Outcomes of imposed non-interventional post-authorisation safety studies-2025/12/2
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Document: Agenda of the CVMP meeting 2-4 December 2025-2025/12/2
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Document: Questions and answers on implementation of the medical devices and in vitro diagnostic medical devices Regulations ((EU) 2017/745 and (EU) 2017/746) - tracked changes-2025/12/2
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Document: Questions and answers on implementation of the medical devices and in vitro diagnostic medical devices Regulations ((EU) 2017/745 and (EU) 2017/746)-2025/12/2
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Document: IRIS guide for applicants - How to create, submit and manage IRIS applications, for industry and individual applicants-2025/12/2
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Document: Agenda of the COMP meeting 2-3 December 2025-2025/12/2
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Document: Agenda - HMA/EMA Annual Data Forum 2025-2025/12/1
2025-12-02查看详情 > -
Page: Clinical investigation of medicinal products in the treatment of Parkinson's disease - Scientific guideline-2025/12/1
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Document: Concept paper on the need for revision of the guideline on clinical investigation of medicinal products in the treatment of Parkinson’s disease-2025/12/1
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Document: Minutes - Management Board meeting: 2 October 2025-2025/12/1
2025-12-02查看详情 >