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Research Integrity

Research & Innovation | Where big ideas ignite.

  • About Us
    • Outreach
    • Ignite Integrity Events & Contest
  • Human Research
    • General IRB Info
    • Human Research Protection Policy Manual
    • For Researchers & Affiliates
    • For IRB Members
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    • IRBNet
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  • Research Integrity /
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  • Regulatory resources
Research Integrity
  • About Us
    • Outreach
    • Ignite Integrity Events & Contest
      • Ignite Integrity Week
      • Ignite Integrity Contest
        • Entry Form
        • Rules & Information
        • Winners
  • 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
  • Research Misconduct
  • Training
    • IRBNet
      • How to Register in IRBNet
  • Contact Us

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

Office Contact Information

  • Location: Ross Hall
  • Room Number: 217
  • Mailstop: 0331
  • Mailing Address: 1664 N. Virginia Street, Reno, NV 89557
  • Phone: (775) 327-2368
  • Directory: Office directory
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University of Nevada, Reno 1664 N. Virginia Street, Reno, NV 89557 (775) 784-1110
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