This article delves into the evolving landscape of the medical device quality management system in Turkey, highlighting the complexities arising from fragmented legal and political environments.

It emphasizes the need for an innovative and comprehensive approach to navigating the system, especially for healthcare professionals and lawyers. Key points covered include the definition of a medical device quality management system (MDQMS), the application of EU regulations in Turkey, labeling requirements, and regulatory bodies overseeing the medical device market. Pi Legal Consultancy is a medial device regulatory consultancy firm in Turkey.

The conclusion stresses the intricate nature of understanding and operating within the medical quality management system in Turkey, with different authorities holding distinct mandates. It also offers expert support from Pi Legal Consultancy, a regulatory consultancy firm specializing in medical devices in Turkey. You can contact us for expert support on medical device regulatory consultant in Turkey.

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