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本帖最后由 beiwei5du 于 2016-7-5 13:08 编辑
House Committee on Energy & Commerce sent a letter to the US Government Accountability Office calling on the oversight office to investigate whether FDA can adequately monitor the manufacturers in India and China, which in the past have had a history of counterfeiting, adulteration, substandard manufacturing and data falsification.
文章(2015年12月)提到最近中印两国的药品质量问题以及FDA对国内外监管力度的不一致,要求GAO(government accountability office)对FDA海外监管至少在两方面进行评估:foreign drug inspctions和FDA‘s foreign offices
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