GMED has certified its first in vitro diagnostic medical devices under Regulation (EU) 2017/746

GMED is pleased to announce that its team has issued its first certificates under the European In Vitro Diagnostic Medical Device Regulation.

Since its designation on August 19^th, 2021, GMED has mobilized its teams to offer in vitro diagnostic medical device manufacturers certification services according to Regulation (EU) 2017/746 for one of the broadest ranges of medical device category designations. Therefore, GMED can assess its customers’ in vitro diagnostic medical devices without any business prospects limitation while supporting their future developments.

The issuance of these first certificates embodies the commitments and investments made by GMED to support and serve its customers and future customers in their certification projects and availability of devices on the market.

GMED thus confirms its ambitions to serve the healthcare industry on a larger scale, to support innovation as well as focusing on patient safety.