In order to further standardize the filing, production and operation of Class I medical devices in the jurisdiction and ensure the quality and safety of medical devices in the jurisdiction, on the morning of July 19, the Market Supervision and Administration Bureau of Chang'an District, Xi'an, held a special rectification meeting for outstanding problems of Class I medical devices. Zhang Dongan, deputy director in charge of Chang'an District Market Supervision and Administration Bureau, pharmaceutical and mechanization supervision department, comprehensive law enforcement brigade, supervisors of relevant market supervision institutes and heads of 7 first-class medical device manufacturers in the jurisdiction attended the meeting.
At the meeting, Hao Section Chief of the Pharmaceutical and Medical Device Supervision Department of the Chang'an District Market Supervision Bureau conveyed and learned the spirit of the second quarter medical device risk consultation meeting of the Municipal Bureau, arranged and deployed the special rectification work of the outstanding problems of Class I medical devices in Chang'an District, and required strict implementation of the document requirements and earnestly carried out self-inspection and inspection.
Deputy Director Zhang Dongan made a speech on the outstanding problems and regulatory risks in the production of Class I medical devices, emphasizing that enterprises shall not exaggerate and publicize false publicity, shall not illegally add excipients, shall not exceed the scope of operation, and shall pay attention to safety production issues, earnestly fulfill the main responsibility of enterprises, and implement effective comprehensive quality control of products and the whole production process. All relevant market supervision institutes are required to increase supervision, increase the frequency of inspections, and establish a long-term supervision mechanism to ensure the quality and safety of medical devices in their jurisdictions.
Editor in charge: Xiaolan