Notable FDA

FDA Seeks OMB Clearance for Medical Device Adverse Event Reporting Program (MedSun)

FDA's submission of the MedSun information collection for OMB review signals continued focus on post-market surveillance of medical devices through structured adverse event reporting. The Food and Drug Administration has submitted a proposed information collection request to the Office of...

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Sources — verify every claim

Health and Human Services Department, Food and Drug Administration · Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Adverse Event Program for Medical Devices: (Medical Product Safety Network (MedSun)) · Oct 8

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