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University of Nevada, Reno Homepage Research Integrity Research & Innovation | Where big ideas ignite.
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  • Regulatory resources
    • Human Research
      • General IRB Info
      • Human Research Protection Policy Manual
        • Policy Manual Definitions Browse the definitions of technical terms in the Policy Manual
      • For Researchers & Affiliates
        • International Research
        • Research in Schools (K-12)
        • University Student Participants
        • Veterans Affairs Research
        • Clinical Research Resources
          • Clinical Trials Project Life Cycle
          • Clinical Trials Study Management
            • Data Safety & Monitoring
            • Sample Data Safety & Monitoring Plan Outline
          • Clinical Trials Contract & Budget
          • (Current Page) Regulatory Resources
            • Clinical Trial Requirements
            • Clinical Trials Investigator-initiated Research
            • Clinical Trial Registration FAQs
            • HIPAA and Human Subjects Research
            • Obtaining Human Research Data Under HIPAA
        • Quality Assurance Review
        • Consent Process Aids
        • Revised Common Rule requirements for informed consent
        • Creating Recruitment Materials
      • For IRB Members
        • Completing a First-rate Review
      • For Research Participants
        • ¿Debo participar en un estudio científico? Information for research participants translated in Spanish

Regulatory resources

The following are regulatory resources for clinical research.

  • Registration and results reporting requirements
  • FAQs on the registry at clinicaltrials.gov
  • Workflow for investigator-initiated research on clinicaltrials.gov
  • HIPAA guidance
  • HIPAA authorization and waiver of authorization flowchart

Research Integrity

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