Service

Since the National Medical Products Administration imposes increasingly stricter requirements on the clinical study of medical devices, the sponsor, CRO and research center pay more attention to the quality management of the clinical study. The Good Clinical Practice (GCP) for medical devices emphasizes that the sponsor is the first person responsible for the quality of the clinical trial. More and more sponsors will voluntarily, or under the request of the research center, hire a third party to perform an independent audit for the quality of the clinical trial. Tigermed-Jyton has a perfect quality management system for clinical trials of medical devices. The quality assurance department is familiar with relevant regulations of medical device clinical study, experienced in quality management, able to comprehensively audit the clinical trial, and is actively providing high-quality audit service for clients.