Holger Kloess is a senior consultant at the QUNIQUE GmbH office in Switzerland, where he is responsible for EU quality and regulatory compliance for medical and in vitro diagnostic devices. He has more than 10 years’ experience in the medical device industry with an excellent Clinical and Biological background and experience with European and US regulatory requirements.
Holger has a Master’s degree in Biology from the University of Osnabrück and is experienced in project management; business planning and strategic management, as well as communication and negotiation.