Changzhou Inspection Branch held an interview with stapler manufacturers
Changzhou has 53 stapler manufacturers, accounting for about 60% of the province. In order to further implement the main responsibility of manufacturers and strengthen the risk prevention and control in the production process of medical devices, Changzhou Inspection Branch organized a collective interview meeting for stapler manufacturers on October 27. More than 100 people including the legal representative, the person in charge of the enterprise and the management representative of the production enterprise attended the meeting.
The meeting reported the special inspection of stapler manufacturers in the city in the early stage, sorted out the key problems and common problems found in the inspection process, analyzed and judged the causes of the problems, main potential risks, and put forward specific rectification requirements and suggestions. The meeting required enterprises to comprehensively identify potential risks, achieve closed-loop management, and ensure product quality and safety.
In the next step, Changzhou Inspection Branch will strengthen supervision and inspection, investigate and deal with violations of laws and regulations, and constantly consolidate the main responsibility of enterprises by means of "face-to-face supervision", "letter of warning", "letter of warning", centralized notification, and individual interview, so as to promote the high-quality development of medical device manufacturers in the city.
The China Medical Device Market Access Guide is a report drafted by the Medical Device Business Department of CIRS Group, which aims to help companies and individuals who want to sell their medical devices to the People's Republic of China and register their medical device products in NMPA. This guideline describes the key definitions, main regulations, authorities and requirements for the full life cycle of medical devices in China, including pre registration preparation, registration process, testing/inspection, clinical evaluation, quality management system and post registration market management.
Medical treatment is one of the three topics of people's livelihood. As an important supporting point of the medical system, the medical device industry has received more and more attention. When the concept of urbanization is gradually emphasized, the market of medical device industry has been excavated.
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