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Products > Health Care Compliance Association > HCCA’s 2006 RESEARCH Compliance Conference
304 Waivers of Informed Consent for Emergency Research: What Can We Learn from PolyHeme®’s Experience?

John Mills, Legal Counsel, Mayo Clinic

  • Outline the legal requirements for an IRB to waive the informed consent requirement for emergency research
  • Discuss the controversy unfolding in the national media related to a study of the blood substitute, PolyHeme®
  • Discuss how the controversy over the PolyHeme® study can help inform the process for future waiver requests

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