Medidee provides expertise in Clinical and Regulatory Affairs for Medical Devices and IVD and assistance for Quality System Management (QMS) implementation. Our services cover all steps of a medical device development, from the initial project idea over the design & development to certification or regulatory clearance. We are located in Lausanne, Olten, Erlangen, Tuttlingen, Lübeck, München, Copenhagen, Aarhus, Ghent, Brussels, Charleroi and Boston.