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      Stem Cell Research Oversight Committee
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Research Administration > Compliance > Institutional Review Board
  • Institutional Review Board
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Guidance

  • Research with Children
    • SOP for Obtaining Consent from Subjects who Enrolled as a Minor  PDF document
    • SOP for Establishing Legal Guardianship for Pediatric Subjects  PDF document
  • Guidelines for Genetic Testing  PDF document
  • Requesting Medical Records from UH for Research Purposes  PDF document
  • Assessing Capacity to Consent for Research  WORD document
  • Policy for Genome-Wide Association Studies (GWAS)
  • NIH web site for: Genome-Wide Association Studies (GWAS)

FDA Guidance

  • Requesting an IND Consult from the FDA  PDF document
  • PI Responsibilities for Research Involving a Significant Risk Device  PDF document
  • In Vitro Diagnostic Device Guidance  PDF document
  • Obtaining Consent in studies using In Vitro Diagnostic Devices  PDF document
  • In Vitro Diagnostic Devices Decision Tree  PDF document
Forms & Documents...
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    • IRB— How to

IRB Information...

  • Meeting Dates/Deadlines
  • IRB Members Restricted Access
  • Information Packet for Study Sponsors Restricted Access PDF document
  • Assurance Information:
    • FWA #00005967
    • IRB Reg. #00000391
    • IORG #0000234

SUNY Upstate Notice of PRIVACY PRACTICES

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