FDA's Final Medical Device Reporting Regulations
نویسندگان
چکیده
منابع مشابه
FDA Regulation of Medical Devices and Medical Device Reporting
There are three main stakeholders in medical device regulation: people in industry, regulators and practitioners. A medical device report is filed after a device-related adverse event occurs. Studies show that while most medical device reports begin with practitioner observations, people in industry file 97% of reports and practitioners file 3% of reports. The objectives of this article are to ...
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ژورنال
عنوان ژورنال: Infection Control & Hospital Epidemiology
سال: 1996
ISSN: 0899-823X,1559-6834
DOI: 10.1017/s0195941700004124