Is specialized in international regulatory affairs for medical devices and in vitro diagnostics. Our core competence is CE-marking for the European market. In addition, we offer a broad range of activities in order to realise your market success.
Based on your individual requirements CE+ supports you in major market-relevant topics such as reimbursement, market access strategies and system building through licensing and partnering.
In doing so resources of our international network will be coordinated in a way that gives you access to the know-how needed for your project. Interdisciplinary teams develop project specific solutions which will lead to outstanding market success.
Trustworthy and straight!
