Beijing FDA made special inspection of medical devices

Perlang Medical News: In order to ensure that the pharmaceutical and medical device products in the market are legitimate and valid, requires not only the legitimate channels of product purchased products placed on the manufacturers and workshop environment has very strict requirements. Recently, Changping Drug Administration work City Medical Device Testing clean environment of Beijing sterile implantable medical device producers launched a special inspection, supervision and inspection and the Beijing the Bai Ren Medical Science and Technology Co., Ltd. as well as the production site clean shop and sterile laboratory environment monitoring. According to the documentation requirements of the Municipal Food and Drug Administration "About eighteen strengthened during the production and use of medical devices regulatory work" Branch actively working with the City Medical Device Testing the communication requirements of the time limit for the completion of the inspection file. Branch of the supervising officer for corporate clean workshop site, production process control, product testing and other aspects of the inspection, the same time, the city is seized by the inspectors of the company's clean shop and sterile laboratory scene detection, no problems found and safety hazard. Inspectors further calculation and analysis of data for site acquisition, it will issue a formal test report.

    After the issue of the report of the test results, Changping branch as required work to complete the results of feedback and response to subsequent processing.