{"id":170,"date":"2020-07-15T07:28:57","date_gmt":"2020-07-15T14:28:57","guid":{"rendered":"https:\/\/www.symaconsulting.com\/blog\/?p=170"},"modified":"2020-07-15T07:30:37","modified_gmt":"2020-07-15T14:30:37","slug":"gmed-designated-under-regulation-eu-2017-745-on-medical-devices","status":"publish","type":"post","link":"https:\/\/www.symaconsulting.com\/blog\/gmed-designated-under-regulation-eu-2017-745-on-medical-devices\/","title":{"rendered":"GMED designated under Regulation (EU) 2017\/745 on medical devices"},"content":{"rendered":"\n<p><\/p>\n\n\n\n<p>GMED official publication on linkedin:<\/p>\n\n\n\n<p>GMED (CE 0459) has been designated as a Notified Body under the Regulation (EU) 2017\/745 by the French National Agency for Medicines and Health Products Safety (ANSM).<br><br>Equipped with this designation since July 8 2020, GMED has mobilized its teams to offer manufacturers with certification services according to the Regulation (EU) 2017\/745 for a field of medical device categories among the broadest.<br><br>Read the full communication: https:\/\/lnkd.in\/datrRVahttps:\/\/www.linkedin.com\/posts\/gmed-north-america_notifiedbody-cemarking-mdr-activity-6686532474765352960-_3V-<\/p>\n","protected":false},"excerpt":{"rendered":"<p>GMED official publication on linkedin: GMED (CE 0459) has been designated as a Notified Body under the Regulation (EU) 2017\/745 by the French National Agency for Medicines and Health Products Safety (ANSM). 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