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FDAnews Device Daily Bulletin
Sept. 11, 2012 | Vol. 9 No. 178
FDA Offers Four-Pronged Plan to Strengthen Postmarket Device Surveillance
In a report released Thursday, the FDA outlined a four-step plan to intensify its postmarket medical device surveillance system. According to the report, “Strengthening our National System for Medical Device Postmarket Surveillance,” the plan is designed to bolster the agency’s efforts to better monitor and report on the effectiveness and safety of medical devices.
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