Medical device Salesforce companies have the essential responsibility of enhancing the lives of patients by providing them with instruments and gadgets. These are intended for injury or disability compensation, chronic... Read More
Tag: Medical Devices
Freyr provides regulatory support to the medical device manufacturers in De-Novo registration of medical devices in the USA that span across classification, Pre-Submission/Q-Submission meeting request, risk benefit determination, De-Novo submission... Read More
Freyr provides United Kingdom Responsible Person(UKRP) services for foreign medical device manufacturers with end-to-end regulatory support for registration and market entry in UK.Freyr provides United Kingdom Responsible Person(UKRP) services for... Read More
Freyr provides regulatory support for medical device manufacturers in 510k submission (510 k premarket notification) to USFDA, which include predicate device identification, 510k application compilation, gap analysis, publishing, creation &... Read More
The printed circuit board (PCB) is a crucial component in the design of medical devices. A well-designed PCB can improve the reliability, safety, and performance of medical devices. However, designing... Read More