CE+ is an associated company of Dr. Regenold GmbH and specializes in international regulatory affairs for medical devices and in vitro diagnostics. The core competence of CE+ is CE marking for the European market as well as offering associated activities to assist clients realize market success.
CE+ is linked with regulanet®, the international network of Dr Regenold GmbH, and therefore able to access resource and manage complex international projects on behalf of clients.
CE+ uses interdisciplinary teams to develop project specific solutions tailored to clients’ needs, helping them maximize value from their asset in the market place.
Visit us: www.ceplus.eu