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2012 SACHRP Recommendations

SACHRP advisory documents are the result of considerable Committee effort, deliberation and consensus building. Once the Committee achieves consensus on an issue, its recommendations are posted on this website and transmitted by the Chair to the Secretary of Health and Human Services, Assistant Secretary for Health, and to the Director of OHRP for their consideration. The content of these documents is advisory and does not represent the official views or policies of OHRP or the Department of Health and Human Services.

March 30, 2012 SACHRP Letter to the HHS Secretary

  • Attachment A: Recommendation on Applicability of FDA Regulations for IRBs
  • Attachment B: Recommendation on Single Patient Treatment Use
  • Attachment C: Recommendation on Protocol Deviations
  • Attachment D: Recommendation Regarding Oversight of Research Misconduct and Regulatory Noncompliance
Content created by Office for Human Research Protections (OHRP)
Content last reviewed June 24, 2021
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