Medical device regulatory work telephone conference kicked off in 2013
Medical equipment exhibition event in between insiders and medical device regulatory work conference is authoritative exchange platform between the regulated community structures. Yesterday, the 2013 National Medical Device Regulatory television and telephone conference kicked off in Beijing, meeting be summarized and affirmation not only of the achievements of the 2012 national medical device regulatory supervision of medical devices in 2013, given the demands and expectations.
It is understood that the main task of the meeting is: to thoroughly implement the spirit of the Party and 18, in accordance with the requirements of the 2013 Food and Drug Management and Clean Government meeting, a comprehensive summary of the 2012 national medical devices regulatory work, deployment the key tasks in 2013, and strive to create a new situation in the medical device regulatory work. Coke red, the State Food and Drug Administration, Deputy Secretary, attended the meeting and delivered a speech.
Coke says that the good supervision of medical equipment in 2013, the overall supervision global implementation of supervisory responsibility. Focused on building a system, improve the regulatory system; reform and innovation as an opportunity to further strengthen the supervision of risk; goal to improve the system, to consolidate the regulatory basis; provide strong support for the protection in order to enhance the technical capacity for the administrative supervision; informatization construction as a means to enhance the effectiveness of supervision and control; fundamental team building, and constantly improve the level of regulation.
If you have any questions, please feel free to contact us.
It is understood that the main task of the meeting is: to thoroughly implement the spirit of the Party and 18, in accordance with the requirements of the 2013 Food and Drug Management and Clean Government meeting, a comprehensive summary of the 2012 national medical devices regulatory work, deployment the key tasks in 2013, and strive to create a new situation in the medical device regulatory work. Coke red, the State Food and Drug Administration, Deputy Secretary, attended the meeting and delivered a speech.
Coke says that the good supervision of medical equipment in 2013, the overall supervision global implementation of supervisory responsibility. Focused on building a system, improve the regulatory system; reform and innovation as an opportunity to further strengthen the supervision of risk; goal to improve the system, to consolidate the regulatory basis; provide strong support for the protection in order to enhance the technical capacity for the administrative supervision; informatization construction as a means to enhance the effectiveness of supervision and control; fundamental team building, and constantly improve the level of regulation.
If you have any questions, please feel free to contact us.
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