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Human Research Protection Program Office of Research Regulatory Support

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A-Z Help Topics

Need help or information about a particular topic? This page has been created to help share and link to information on topics related to human subject research protection.

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  • Anonymous and De-identified Data
  • Certificate of Confidentiality
  • Click (TM) Research Administration Help Guides and Videos
  • Clinical Research Billing Compliance
  • Conflict of Interest
  • Consent Form Guidelines
  • Consent Form Key Information Guidance
  • Definitions
  • Exempt Categories
  • Expedited Categories
  • Graduate Student Research
  • HIPAA
  • HIPAA and MSU Health Care, Inc.
  • Individual Investigator Agreements
  • Investigational Drug Accountability
  • Investigational Drugs and Devices Storage and Handling
  • Investigator Responsibilities
  • Multi-Site Research
  • New Faculty Information
  • NIH Single IRB
  • Non-Exempt Studies with No Expiration Date
  • Pregnancy testing when Research Involves Non-Contrast MRI of the Head
  • Principal Investigator Requirements
  • Protected Health Information
  • Quality Assurance, Improvement, and Program Evaluation
  • Record Retention
  • Reliance Process
  • Reliance Partner Institutions
  • Reportable Events
  • ResearchMatch
  • Revised Common Rule Single IRB Requirements
  • Single IRB Requirements
  • Site Visits
  • Templates (required forms for submissions, informed consent templates)
  • Training

Help & Requirements

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  • Review Types & Process
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  • Revised Common Rule
  • FAQs
  • A-Z Help Topics

About HRPP

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