FDA Submits Proposed Collection of Information for Adverse Event Reporting and Recordkeeping of Dietary Supplements

Summary

The Food and Drug Administration (FDA) has submitted a proposed collection of information to the Office of Management and Budget (OMB) for review and clearance, as required by the Paperwork Reduction Act of 1995, in order to implement adverse event reporting and recordkeeping requirements for dietary supplements under the Dietary Supplement and Nonprescription Drug Consumer Protection Act.