Product tests are an essential part of the evidence management within the framework of the CE conformity assessment procedure according to the EU Medical Devices Regulation (MDR) or also in the application procedure for HMV-listing. In addition to the selection and sequence of the tests, the selection of the testing institute is also an essential aspect for the official recognition of the test certificates. As we often have to apply very specific procedures in medical technology, a certain amount of experience in planning and implementation is required; benefit from our expertise. We organise and supervise your testing.
We support you with our network in researching and carrying out tests. BEO BERLIN helps you to find efficient partners at eye level and accompanies you through the necessary steps.
