WASHINGTON, May 9 (TNSFRinfo) -- The U.S. Department of Health and Human Services Food and Drug Administration (FDA) is requesting public comment on its proposed collection of information regarding medical device reporting. This process, mandated under the Paperwork Reduction Act of 1995, allows the agency to gather essential data on adverse events and malfunctions associated with medical devices from user facilities, manufacturers, importers, and distributors. The FDA utilizes this information . . .

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