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University of Nevada, Reno Homepage Research Integrity & Security Research & Innovation | Where big ideas ignite.
  • Program Areas
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    • Program Areas
      • Human Research
        • General IRB Info
        • Human Research Protection Policy Manual
          • Policy Manual Definitions Browse the definitions of technical terms in the Policy Manual
        • Quickstart Guide for Researchers
          • International Research
          • Research in Schools (K-12)
          • University Student Participants
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          • Clinical Research Resources
            • Clinical Trials Project Life Cycle
            • Clinical Trials Study Management
              • Data Safety & Monitoring
              • Sample Data Safety & Monitoring Plan Outline
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            • (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
      • Institutional Animal Care and Use Committee
      • Institutional Biosafety Committee
      • Conflict of Interest
        • Disclosure Instructions
        • Procedures
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          • Reviewing Requests
          • Navigating COI and Related Regulations
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        • Paid Travel
        • Impacts on Students
        • Conflict of Interest Training
      • Responsible Conduct of Research
      • Research Misconduct
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      • U.S. Export Controls
        • Overview of Regulations
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          • Research Compliance
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        • Protecting Electronic Data During Travel
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        • Publicly Available, Public Domain, Open Source
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Announcement: The federal administration has enacted a number of Executive Orders that have implications for federal proposals and awards. View more information on research activity impacts.
  • University Homepage
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  • Research Integrity /
  • Program areas /
  • Human research /
  • Quickstart guide for researchers /
  • Clinical research resources /
  • Regulatory resources
    • Program Areas
      • Human Research
        • General IRB Info
        • Human Research Protection Policy Manual
          • Policy Manual Definitions Browse the definitions of technical terms in the Policy Manual
        • Quickstart Guide for Researchers
          • 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
      • Institutional Animal Care and Use Committee
      • Institutional Biosafety Committee
      • Conflict of Interest
        • Disclosure Instructions
        • Procedures
        • Outside Compensated Services
          • COA Request Instructions
          • Reviewing Requests
          • Navigating COI and Related Regulations
        • Financial Conflicts of Interest
        • External Relationships
        • Paid Travel
        • Impacts on Students
        • Conflict of Interest Training
      • Responsible Conduct of Research
      • Research Misconduct
      • Research Security
      • U.S. Export Controls
        • Overview of Regulations
        • Policies and Procedures
          • Research Compliance
          • International Shipping
          • Foreign Workers and Visitors
          • Restricted Party Screening
          • Licensing
          • Recordkeeping Requirements
          • Reporting Violations
        • Protecting Electronic Data During Travel
        • Laptop Loan Program
        • Deemed Exports
        • Publicly Available, Public Domain, Open Source
        • Educational Information
        • Fundamental Research Exclusion
        • International Travel & Data Protection
        • Export Controls Training
      • Effort Reporting
        • Effort Certification
        • Working with Salary Caps
        • Video Tutorials

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 & Security

1664 N. Virginia Street, Reno, NV 89557
Ross Hall 217, Mail stop: 0331
(775) 327-2368

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