Guide destiné aux promoteurs pour la procédure synchronisée des études combinées CTR–MDR/IVDR

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Guidance for sponsors on the synchronised procedure for combined CTR–MDR/IVDR studies Belgium offers a synchronised submission procedure for combined studies involving medicinal products and medical devices and/or in vitro diagnostic devices. This Belgian approach aligns the timelines of both submission procedures, making it easier and more efficient for sponsors to submit their applications. …

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Federal Agency for Medicines and Health Products (FAMHP) — imported from official source
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October 03, 2026 20:37
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110391 at https://www.famhp.be

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