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Human Research Protection Program Office of Research Regulatory Support

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FAQs

Included below is an index with links to specific Frequently Asked Questions (FAQs) pages. The specific FAQ pages have been organized by topic.

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  • Clinical Research Billing Compliance
  • COVID-19 and Human Research Protection
  • Data Security
  • HRPP Training
  • IRB Review Process
  • Reliance
  • Revised Common Rule
  • Training 

Help & Requirements

  • Activities Requiring Review
  • What & How to Submit
  • Review Types & Process
  • Federal, State, Local Requirements
  • HRPP Manual
  • Revised Common Rule
  • FAQs
  • A-Z Help Topics

About HRPP

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  • About Us
  • IRB Committees

ORRS Units

  • Animal Care Program (IACUC, CAR)
  • Conflict Disclosures and Management (CDM)
  • Environmental Health & Safety (EHS)
  • Export Control and Trade Sanctions (ECTS)
  • Stem Cell Research
  • ORRS Information & Communication Technology
  • ORRS Administration

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