Device suppliers to UK must heed new tissue rules
This article was originally published in Clinica
Executive Summary
The UK's Medical Devices Agency has become the first regulatory authority in the EU to issue guidelines on standards for organisations supplying the health service with medical devices using material of human origin. The UK is reacting to an urgent need for some sort of regulation in this area while awaiting official regulatory developments at the European Commission (see above), which have been slow.
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