Business · 17/08/2006Updated: 10/17/2026 · 1 min read
FDA Announces Approval of MedWatch Information Collection for Partners Organizations
Summary
The Food and Drug Administration (FDA) has received approval from the Office of Management and Budget (OMB) to collect information from MedWatch partners organizations under the Paperwork Reduction Act of 1995, as part of the MedWatch Safety Information and Adverse Event Reporting Program.
Original source language: Federal Register — Food and Drug AdministrationOpen original release →