Medical Device Reporting Program: Sample Policy

December 13, 2017 | Healthcare Risk, Quality, & Safety Guidance

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​A medical device reporting program identifies medical-device-related incidents as soon as possible after their occurrence in order to initiate corrective acti​on, prevent or minimize the occurrence of similar incidents, and comply with the reporting requirements of U.S. Food and Drug Administration regulations and the Federal Food, Drug, and Cosmetic Act.

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