The IRB

• Survey Results
  
  
• See What’s New, including:
  
  
  • OHRP's 2015 edition of the International Compilation of Human Research Protections.
    
    
  • Guidance on Genomic Data Sharing and FAQs - for NIH grant submission.
    
    
  • Recruitment guidance updated - a 'must read' for researchers!
    
    
  • CITI training - existing records have been converted
    to use SUNet ID and password as CITI log on information (not applicable to VA users.) See CITI (Tutorial).
    
    
  • Closing a protocol FAQs.
    
  
  
  

Quick links for researchers

Getting started For Researchers Determination of Human Subject Research (HSR) (get IRB decision if HSR)

Consent Templates, Forms, eProtocol attachments Medical - consents, minimal risk samples, short form Nonmedical - consents, parental permission Medical & Nonmedical - assent, phone scripts and screens, etc. eProtocol Required Attachments (VA, international research, etc.) Sample eProtocol Applications

FAQs About eProtocol Human subjects training Before submitting a protocol (what you need to know) What to consider when submitting a protocol After approval (ongoing submissions to the IRB) Expanded Access (Expanded Access, Emergency Use, Humanitarian Use) Working with Central and External IRBs (CIRB)

• About the IRB (the Administrative Panels on Human Subjects Research)
  
  
• Charge to the IRBs