The medical device industry thrives on innovation. With innovation in medical technologies comes the responsibility of safety, and new medical devices must conform to strict safety requirements as set out by regulatory bodies, such as the FDA. Technical guidance for the specific in vitro mechanical tests to meet the regulatory requirements is generally provided by the ISO and ASTM. Zymetrix will work with you to navigate the technical requirements for your specific device. Compliant with Good Laboratory Practices, Zymetrix has both the equipment and the processes in place to ensure the quality of your data and reporting.