The eighth China International Medical Device Regulatory Forum (CIMDR) was inaugurated on August 16, 2017 in Hangzhou. Jiao Hong, the deputy director of China Food and Drug Administration (CFDA), attended the meeting and made a speech.
Jiao Hong, Deputy Director of CFDA, gave the instruction
Jiao Hong pointed out that over the years, the innovation of global medical devices has been undergoing rapid development and has become an important force to lead the transformation of medical models and drive medical progress in diagnosis and treatment technology. CFDA carries on its shoulders the important mission of guaranteeing the safety of medical devices used by the people, and actively pushes forward the reform of the evaluation and approval system for medical devices. It has made promising achievements in aspects such as improving the quality and efficiency of the evaluation and approval and encouraging the innovation and research for new products and new technologies. Next steps would be proceeding to deepen the reform, reinforcing the management of the full life cycle of medical devices, ensuring that enterprises fulfill their legal liabilities in the full process full lifecycle covering design and development, clinic test, production and sales, product recall and report on negative incidents, and effectively guaranteeing the safety of medical devices.
The Forum was sponsored by China Center for Food and Drug International Exchange (CCFDIE) and organized by Center for Medical Device Evaluation. The Forum has been held for 8 sessions and is becoming increasingly influential. It built an amazing platform where supervision policies and experiences for medical devices in China and in other countries are shared, information on innovative development of the industry is exchanged and friendship is strengthened, and playing an important role in international communication and cooperation in China in the field of medical device supervision and driving the innovative development of the medical device industry.
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