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  • The eighth international conference on Chinese medical devices is held in hangzhou
  • Release time: 2017-08-17 Clicks:1732 
  •  On August 16, the eighth international conference on the supervision and management of medical devices in China opened in hangzhou. National food and drug administration bureau of food and drug administration, the vice bureau of the general administration, attended the meeting and spoke.
    Jiao hong pointed out that, in recent years, the innovation of medical devices in the world has been developing vigorously, which has become an important force leading to the transformation of medical model and the advancement of medical diagnosis and treatment technology. Food and drug supervision bureau for the important mission to protect the safety of the people by machinery, actively promote review of medical equipment examination and approval system reform, the promotion review for examination and approval of the quality and efficiency, encouraging new product research and development of new technology innovation achieved positive results. The next step will continue to deepen reform, strengthen the whole life cycle management of medical equipment, the implementation of the enterprise for the design and development, clinical trials, production and sales, product recalls, adverse event reports of whole life cycle of the whole process of legal responsibility, and to ensure the safety of medical equipment.
    During the meeting, the administration of medical device registration division, medical equipment and supervision, kaohsiung, the pipe center, evaluation center, careful interpretation and complaint reporting center, head of the Chinese medical device regulatory policy and international cooperation. The relevant officials from the United States, Ireland, Saudi Arabia, Japan and other countries and regions in the regional medical device industry have elaborated the progress of the supervision of the relevant national and regional medical devices. Experts from Chinese and foreign industry have exchanged understanding and practical experience on global regulatory legislation. In addition to the general assembly, the meeting also hot issues around the industry set up a medical instrument BBS clinical trials and post-marketing surveillance of medical equipment and verification BBS, risk management and medical devices adverse events monitoring biological evaluation BBS BBS, medical equipment, medical equipment innovation technology and products, such as BBS BBS 16 points. Representatives from Chinese and foreign medical device regulators, technical institutions and more than 700 representatives from industry attended the meeting.
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