A class of medical device clinical trial requirements

First of all, the filing of applications must be within the municipal jurisdiction and registered enterprises in accordance with the law, followed by a class of medical devices to have the enterprise's record certificate, including the production site, production equipment and dedicated page and other relevant proof, but also need to have the production of a class of medical device products, equipment, and storage space, is the need to apply for the production of a class of medical devices in line with national standards.