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Page: Frequently asked questions-2025/3/14
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Document: Frequently asked questions (FAQs): How to create, submit and withdraw a Clinical Trial Application - CTIS Training Programme - Module 10-2025/3/14
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Document: User guide for micro, small and medium-sized enterprises-2025/3/14
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Document: Product Management Service (PMS) roadmap-2025/3/14
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Page: Network Portfolio-2025/3/13
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Document: Release notes - production release version 1.7.2514 - 12 March 2025 - Veterinary Medical Products Regulation: Union Product Database-2025/3/13
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Document: Network Portfolio Roadmap-2025/3/13
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Page: High-risk medical devices: consultation procedures and advice-2025/3/13
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Document: List of clinical evaluation consultation procedure (CECP) opinions issued for medical devices awaiting finalisation of conformity assessment-2025/3/13
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Document: Drug-Eluting stent (DES) - Notified Body 2265 - 10/01/2025 - Expert decision and opinion in the context of the clinical evaluation consultation procedure (CECP)-2025/3/13
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