Zdrowie i gospodarka · 19/01/2023

FDA Solicits Public Comments on Proposed Adverse Event Program for Medical Devices

The Food and Drug Administration (FDA) is requesting public comments on its proposed collection of information related to the Adverse Event Program for Medical Devices, also known as the Medical Product Safety Network (MedSun). The FDA must publish this notice under the Paperwork Reduction Act of 1995 and allow 60 days for public comment.