The EU medical devices MDR is made to overlook the labelling, requirements, establishment, production, and registration of devices for avoiding the risk involved.Under these regulations, the government ensures the quality and safety of devices to customers.For more information, visit our website.
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Established in 2016, the Company coordinates activity in a wide variety of fields providing complementary professional services for customers of the medical and civil sector, in Israel and abroad: consulting, medical device development services, documentation, maintenance, clinical trials, manufacturing and more.
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Medical device regulation is a framework to analyze the risk involved in using the devices.It involves the registration of devices, manufacturer's claim CE marking on devices and enhance traceability.For getting more information, visit the website.
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Medical devices MDR in Europe is set by the government in which they will check the quality of products, the performance of devices, safety issues and benefit-risk of these products.Check out the website for further information.
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Israel
www.mdm-projects.com/