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European Medical Device Regulation 2017/745

GMED North America, Inc.

Monday, May 6, 2019 at 8:30 AM - Tuesday, May 7, 2019 at 5:30 PM (EDT)

European Medical Device Regulation  2017/745

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Monday, May 6, 2019 at 8:30 AM - Tuesday, May 7, 2019 at 5:30 PM (EDT)

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GMED North America, Inc.

 GMED North America is the US subsidiary of GMED, the leading French Notified Body (CE0459), part of the LNE group, and an Accredited Certification and MDSAP Recognized Organization. 

We serve the medical device industry worldwide with offices in Europe and the United States. Our goal: Provide the best in Product Certification and Quality Management Services  through CE marking, ISO 9001:2015, ISO 13485:2016 and MDSAP.


With a long tradition in providing testing services like EMC and electrical safety testing for any of the European medical device standards, we also offer a full range of technical conformity services, from diagnostic audits to training, allows the convenience and efficiency of a local based team of technical experts, auditors and program managers and make us one of the leading European Notified Body.

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