Xishan District convene the annual meeting of the Medical Device business executives

Grades of a mechanical products as drugs and medical devices on the importance of the people, and therefore do a good job medical device regulatory became the important work of the Drug Administration Department. Xishan District, Wuxi City Medical Device regulatory work to achieve greater performance, the Food and Drug Administration recently convened a special meeting the region's pharmaceutical retail corporate governance and enterprise responsible person annual meeting. Conference to sum up the 2012 regulatory reporting, and deployment of the 2013 Medical Device circulation regulatory tasks, will comprehensively improve supervision.

2012, Xishan Bureau of efforts to strengthen the scientific supervision, exploratory carry gridded supervision of drug retail enterprises GSP remote monitoring system online rate remains above 95%, the number of reports of adverse drug reactions per million population 365, Medical equipment Adverse incidents, the national medical Device Adverse Event Monitoring Network online reporting unit 153 to report the number of adverse event reports 644 cases per million population, indicators rank the forefront of the city.


    2013, Xishan will create drug safety demonstration area as the starting point, active and innovative regulatory approaches, prominent the remote supervision gridded regulatory and credit supervision, and implementation of the norms of good patches of grid management, and actively strengthen the credit system construction, vigorous efforts should be easy to precursor chemicals containing ephedrine special inspection, special inspections of Chinese Herbal Medicine, Drug adverse reactions, medical product adverse events reported to work, improve the level of supervision of the field of pharmaceutical distribution.

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