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Eu Medical Device Regulations Services
3 services found
Manufactured by:Egemen International based inIzmir, TURKEY
PMS (Post Marketing Surveillance) activities consist of a process in which the performance and safety of medical devices are continuously monitored after the supply of products to the market. The necessity for post-market monitoring of a medical device begins immediately after the medical device is placed on the ...
Manufactured by:Avania based inBrunswick, AUSTRALIA
All businesses are unique - consistency and reliability are critical to ensuring quality. Whether you are part of an emerging company or a long-established multinational corporation, Avania can ensure your quality system fits your organizational ...
by:in2being, LLC based inSaline, MICHIGAN (USA)
All medical devices in the United States are regulated by the Food & Drug Administration (FDA), and understanding the FDA’s definition of a medical device as well as how the agency classifies medical devices is a crucial part of learning how to bring your medical device to ...