In addition to accredited and established test procedures, we also carry out literature reviews on the current state of science and technology based on publications and applicable standards for testing services.
Especially with regard to the new medical device regulation EU MDR 2017/745, pre-clinical data are required for the verification and validation of medical devices (Annex II, paragraph 6.1), which include test results as well as an evaluation of the current scientific literature.

We offer appropriate research on test methods and their results in international literature and advise on corresponding test services in our company.