Regulation Countermeasures Of Handan Medical Equipment Circulation Market

Medical devices are a special class of commodities that are used to protect the life andhealth of the masses to, involving multiple disciplines of medicine, machinery, electronics,biotechnology, testing, etc.. Medical devices are a multi-disciplinary, knowledge-intensive,capital-intensive and high-tech products. With the deepening of reform and opening up, thecontinuous increase state support and accelerate the process of global integration, the Chinesemedical device industry has been through a rapid development, making medical devices havebeen widely used in disease prevention, diagnosis, treatment, care and rehabilitation and playan increasingly significant role in the process of people’s lives. While the recent "polyacrylamide hydrogel "," US-pupil affair" mass accidents, so that safe and effectivemedical devices become publicly concerned. Although the industrial development of China’smedical equipment faster, because of the late start time, imperfect institution-building, itcaused some medical device companies a sense of responsibility, integrity and consciousness,fraud, illegal operation. It resulted in a big security risk within medical equipment distributionmarket. Therefore, it is meaningful to study effective policy in order to solve the problemassociated with the distribution of medical devices.Based on the status of medical equipment distribution market and the emergence ofHandan City, the regulatory process at the grassroots level of difficulty and blind analysis,this thesis summarized the main problems the city medical device market circulationregulatory regime exists. Deep reasons were analyzed, in order to find a countermeasure tosolve these problems. This study is conducted based on the current city medical equipmentmarket supervision work practices, comprehensively and objectively investigate and corporateself-discipline supervision of medical devices exist weak; regulators to limit the level ofprofessional skills; inadequate technical support forces; lag monitoring of adverse events; thelack of regulation of medical devices; imperfect legal system and other issues, and one byone in-depth analysis, on this basis, by summing up the experience of mature foreign medicalsupervision reference proposed strengthen self-discipline; improve their professional skills, establishment of high-quality team; improve technical support forces, the establishment ofthird-party testing organizations; innovative regulatory approach, exploring regulatory model,strengthen risk management, good adverse event monitoring, improve the legal system andother six countermeasures for market surveillance of medical devices in circulation soundsystem and the protection of the safety of medical devices, to provide a referenceeffectiveness, building a science, improve medical device market regulatory system, toachieve scientific supervision, and promote the healthy development of medical equipmentdistribution market, to protect the masses with firearms safe and its effectiveness.