New service: advice on preclinical data

Especially with regard to the new, Europe-wide medical device regulation EU MDR 2017/745, pre-clinical data is required for the verification and validation of medical devices (Annex II, paragraph 6.1), which can include test results and an evaluation of the current literature.
We offer appropriate research on test methods and their results in international literature and advise on corresponding test services in our company.

Get more information under "Consulting".