|A CE mark is not simply mandatory for the European market, it is also an advantage with respect to markets outside of Europe, where it is widely recognized as a quality mark. We intend to open doors for our customers to new markets and additional international registrations. For that reason, we offer the following international certifications in collaboration with our cooperation partners:
– certification according to MS ISO 13485
– certification according to GDPMD (Good Distribution Practice for Medical Devices)
– Technical File Review
MEDCERT grows with its customers – our goal is to offer you all certifications crucial for your export activities and registration of your devices in other countries. Are you interested in a certification according to one of the above mentioned standards? Then please send us back the completed quesstionaire.