MEDTEQ Testing Services
The MEDTEQ facility has a medium range of test equipment as detailed below for testing to various standards. MEDTEQ reports have the equivalent status of a manufacturer's report, which is acceptable under medical device regulations for many regions, such as US, Europe, Canada and Australia. The reports contain a cover page, general description, sample identification (including photos), clause list (core evaluation), and test data. Unlike CB scheme reports, the test data section is a self contained record for all items inspected, measured or tested, with full details such as test engineer, sample identification, testing dates, environment, test equipment and methods used. This detail provides confidence for regulatory auditors.
