provides support for all regulatory and quality management issues in medical technology. Our global team covers the majority of country approvals and can participate in many fields. These include ISO13485, 2017/745 MDR , 2017/746 IVDR, US FDA software, electrical safety, EMC, clincial evaluation and many other topic.

Solutions & Services

We help you with all matters concerning the placing on the market of your medical devices according to MDR.

according to ISO 13485

according to ISO 14971

Professional advice for Medical Devices and Life Science

“In MedTech and Lifescience it is simple: Compliance means business and no compliance means no business”

Stefan Bolleininger

Call: +49 9123 1529250

Office adress, Visitors adress, Büroanschrift:
be-on-Quality GmbH
Bahnhofstrasse 85
91233 Neunkirchen am Sand

Headquarter of  be-on-Quality GmbH
Lilienstrasse 33, 91244 Reichenschwand