Business · 18/01/2024Updated: 10/17/2026 · 1 min read

FDA Announces Approval of Institutional Review Board Waiver for Minimal Risk Clinical Investigations

Summary

The US Food and Drug Administration (FDA) has announced that it has received approval from the Office of Management and Budget (OMB) to collect information related to Institutional Review Board Waiver or Alteration of Informed Consent for Minimal Risk Clinical Investigations under the Paperwork Reduction Act of 1995.

Original source language: Federal Register — Food and Drug AdministrationOpen original release →

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