Head of Consulting, Quality Management & Regulatory Affairs
Peter Hartung studied precision engineering at the Technical University of Dresden from 1989 to 1994.
The he worked for eight years in a company that develops and manufactures mobile chemical analysis technology.
Here he worked in the field of design, hardware and software development and was responsible for the production and approval of the products.
After entering seleon GmbH in 2002, he took over the mechanical development department for two years. As project manager, he was responsible for the development and approval of innovative medical devices.
From 2004 to 2014, Peter Hartung led the Quality Management & Regulatory Affairs department and, since 2014, the Consulting business unit.
He is responsible for the development, manufacture and approval of a wide range of medical devices in compliance with requirements at seleon and the customers he advises. He has extensive experience in setting up medical technology companies and coaching in the areas of quality and process management, regulatory & clinical affairs and life cycle management.