Medical Device Reporting Program: Sample Policy

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


​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.

Access Full Content

Contact us today at 610.825.6000.