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最近,政府审计局(GAO)的一份报告指出,FDA接收制造商使用医疗仪器反向经验报告的制度存在问题。来自GAO调查监督委员会的报告列举了被医院和制造商低估
Recently, a report from the Government Audit Office (GAO) pointed out that the FDA has received problems with the system of manufacturers’ use of medical devices’ reverse experience reports. The report from the GAO Investigation and Oversight Committee cited the underestimation by hospitals and manufacturers