Ce Plus
CE plus is an international service provider for medical devices and in-vitro diagnostics, based in Badenweiler, in the immediate vicinity of Freiburg and Basel. Our core competence is CE-marking for the European market. Whether undergoing a CE marking process or other international registration procedure, you will need a number of satellite activities in order to meet all needed requirements, e.g. extensive quality and risk management systems. We offer a broad range of activities in order to realize your market success. In doing so resources of our international network will be coordinated in a way that provides you access to the know-how needed for your project. Interdisciplinary teams develop project specific solutions which will lead to outstanding market success. For more information please visit: Legal Notice:
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8 contacts with verified email or phone · masked until revealed.
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Felix Metzner
Senior Regulatory Affairs Expert Non-active Medical Devices · Manufacturing & Production
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Thomas Haszprunar
Regulatory Affairs Manager · Operations
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Sohaib Ahsan
Regulatory Affairs Expert · Science
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Rick Wiegand
Ä - Ä Ü · Other
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Tobias Bartl
- - Ä · Other
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- 2senior regulatory affairs expert non-active medical devices
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