CE plus is an international regulatory service provider for medical devices and in-vitro diagnostics, based in Badenweiler, in the immediate vicinity of Freiburg/Germany and Basel/Swiss. CE plus was founded in 2009 starting with profound operational experience in medical device and IVD industry as well as Notified Body business. With our dynamic
Domain | ceplus.eu |
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Homepage URL | http://www.ceplus.eu |
Keywords | medical devices regulatory affairs strategy market access in-vitro diagnostics combination products companion borderline mdr ivdr quality management system qms clinical evaluation performance investigations post-market studies surveillance biocompatibility biological safety preclinical device software mdsw lifecycle processes cybersecurity |
Sprache | englisch |