Tianjin training equipment related laws and regulations

Recently, the Tianjin Municipal Market and Quality Supervision and Management Committee held a training course on medical device regulations. More than 100 medical device supervisors attended the training.

It is reported that the training takes the form of a combination of theoretical study and case discussion, focusing on the laws and regulations and professional knowledge such as the “Measures for the Management and Re-evaluation of Medical Device Adverse Events” and the “Quality Management Standards for Medical Device Production”, and questions raised by the participants. Discuss and answer one by one. Through training, the ability of grassroots supervisors to discover problems in the production, operation and use of medical devices and the actual inspection level have been improved.