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Page: Plasma master file certificates-2025/1/6
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Document: Mysimba Article-20 procedure - Timetable for the procedure-2025/1/6
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Page: Submission deadlines for orphan designations-2025/1/6
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Document: Deadlines for submission of applications for orphan medicinal product designation to the EMA and corresponding COMP timetable for valid applications - 2024-2025-2025/1/6
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Document: Organisation chart: Information Management-2025/1/6
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Page: Fees payable to the European Medicines Agency-2025/1/6
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Document: Annex to interim measures regarding notification of pharmacovigilance alerts by marketing authorisation holders under Regulation (EU) 2019/6: contact points-2025/1/6
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Document: QRD veterinary combined label-leaflet template v.9.1-2025/1/6
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Document: IRIS guide for applicants - How to create and submit scientific applications, for industry and individual applicants-2025/1/6
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Document: Work plan for the Committee for Veterinary Medicinal Products (CVMP) Efficacy Working Party (EWP-V) 2025-2025/1/6
2025-01-07查看详情 >