seleon GmbH
Karin Berndt has extensive experience in regulatory affairs and quality management, currently serving as Teamleiterin Regulatory Affairs and Senior Consultant QM & Regulatory Affairs at seleon GmbH since October 2019. Prior to this role, Karin held the position of Senior Manager Regulatory Affairs at CRO Kottmann from August 2018 to August 2019. Karin's career began at PAUL HARTMANN AG, where a tenure lasting from August 1995 to July 2018 culminated in the role of Regulatory Affairs Manager.
seleon GmbH
High-Class Medical Technology - innovative, reliable, convincing seleon GmbH has been a leading service partner for medical technology companies in Central Europe for over 20 years, focusing on the areas of development, production and consulting. We develop first-class medical products on the basis of a pronounced innovative strength and technological ambition, thus providing sustainable added value for our national and international customers. Our company, headquartered in Heilbronn, Germany, supports medical technology companies, regardless of size, with their active and non-active medical devices, in-vitro diagnostics and combination products (medical devices & pharmaceuticals) and offers solutions tailored to the requirements of our customers.