Team AB created for devices

Team AB The UK Association for Medical Device Approved Bodies, or Team AB, has been formally launched with the aim of helping industry participants navigate new regulatory requirements.

Team AB will represent U.K.-approved bodies for medical devices and in vitro diagnostics (IVDs) in their dealings with the Medicines and Healthcare products Regulatory Agency (MHRA), which regulates the U.K. medical devices market, as the agency works to create a post-Brexit framework for the sector.

The group will provide a forum for applicants and designated approved bodies to share experiences and facilitate consistency in regulatory understanding and feedback, given the anticipated evolution of U.K. medical device regulations.

To find out more, CLICK HERE.

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