The medical device sector presents with an extremely broad spectrum of continuous innovation, including hundreds of different technologies and a whole universe of types of products in the fields of prevention, diagnosis, therapy, after-care, rehabilitation and nursing care. At the same time, regulatory requirements for placing medical devices on the market, and thereby the need for clinical data, will become substantially more demanding.
Our experienced team of specialists has completed a high number of clinical studies spanning a wide variety of medical devices with or without CE mark.
We have performed international first-in-man and first-in-patient studies.
If you are looking for an expert team guiding your innovative medical device through the increasingly demanding clinical study framework, get in touch with us