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Page: Stability testing for applications for variations to marketing authorisation - Scientific guideline-2025/12/12
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Document: Guideline on stability testing for applications for variations to a marketing authorisation - Revision 3-2025/12/12
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Document: Highlights - 20th EMA Industry Platform meeting on the operation of EU pharmacovigilance legislation meeting-2025/12/11
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Document: Members of the Coordinating group of European network of paediatric research at the European Medicines Agency (Enpr-EMA)-2025/12/11
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Document: Agenda – Executive Steering Group on Shortages and Safety of Medicinal Products (MSSG) (17 December 2025)-2025/12/11
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Document: From laboratory to patients: How the safety of medicines is ensured in the European Union-2025/12/11
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Document: Methodology European Specialised Expert Community (ESEC): Members-2025/12/11
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Document: Methodology Working Party (MWP) interested parties meeting report, September 2025-2025/12/11
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Document: Consolidated 3-year work plan for the Emergency Task Force (ETF)-2025/12/11
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Page: Questions and answers on post approval change management protocols - Scientific guideline-2025/12/11
2025-12-12查看详情 >