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Commission nominates testing bodies under Swiss/EU MRA (mutual recognition agreement)

This article was originally published in Clinica

Executive Summary

The European Commission has published a list of six testing and certification authorities based in Switzerland that are now authorised to audit companies against the requirements of the EU medical device directives. Alongside that list are the names of those notified bodies in the EU which are now recognised as conformity assessment bodies (CABs) which can test products against the requirements of the Swiss laws.

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