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Medical Device Regulation Requirements (MDR)

31.05.2024
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Paylaş :
Medical Device Regulation Requirements (MDR)

Training The training will provide a foundational understanding of the regulatory requirements for Medical Devices (MDR (2017/745/EU)). It will enable personnel, including top management, working as managers or project members in departments such as QM/QA, R&D, design, production, supply chain, customer service, and sales, to comprehend the demands of subcontractors, suppliers, OEMs, authorized representatives, importers, and distributors.

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