The key clinical trials every medical device must undergo before being approved for use on patients call for highly specialised teams and an individualised approach. Pre-requisites which are fundamental components of EXCELYA’s DNA offering a rare quality of proficiency built up over more than two decades of experience in the field of clinical validation trials covering more than 25 countries.
This highly customized protocol enables us to accelerate the medical device validation procedure for our clients in a way they cannot find elsewhere. An objective achieved by drawing upon our extensive technical and therapeutic insight related to regulatory requirements for earning approval. A wealth of expertise backed by the appropriate study design options and safety reporting as well as the endpoint data essential for successfully completing a trial. On time and on budget!
All of which clearly demonstrates why our full clinical trial service is so comprehensive and dependable – all the way to certification and to market.