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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