2) New Submission Forms

All submitted documents must be SINGLE SIDED.

Click on documents to view:

• DFCI Protocol Front Sheet *REVISED*
  • Guidance on Completing Protocol Front Sheet
• New Project Application Forms:
  • Clinical Trials *REVISED*
    • Radiation Safety Protocol Screening Form
  • Social/Behavioral Research *REVISED*
    • Helpful Resource: Guidelines For Writing A Social/Behavioral Science Research Protocol
  • Medical Record Review *REVISED*
    • Helpful Resource: Guidelines For Writing A Minimal Risk Research Protocol
  • Research Use of Human Material/Tissue *REVISED*
  • Request for Exemption or Determination that Activity is Not Human Subject Research 
    • Helpful Resource: OPRS Information Sheet: Determining if Project is Human Subject Research
  • Request for the DFCI IRB to Cede IRB Review

• New!  Alert Page Template
  • Guidance on Alert Pages
    
    
• Statement of Investigator Form for New Applications *REVISED*
  
  
• Co-Investigator and Research Staff Form for New Applications *REVISED*
  
  
• Instructions for Preparing New Protocol Endorsement Letter
  • a sample letter is available upon request by contacting OPRS at 617-632-3029

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  • Office for Human Research Studies (OHRS)
    • Investigator Resources
    • IRB & SRC Review Documents
    • Forms and Instructions
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        Instructions
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        New Submission Forms
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        Consent Forms
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        Continuing Review Form
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        Post Activation Forms
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        HIPAA Research Forms
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        Federal Forms
    • Resource Guidance and Regulatory Links
    • Alerts/News
    • Agreements
    • ONCPRO and OHRS Submit
    • Presentation and Training Material
    • Contact Info
  • Quality Assurance Office for Clinical Trials (QACT)
  • Clinical Research Unit (CRU)
  • Clinical Trials Education Office (CTEO)
  • Protocol Review and Monitoring System (PRMS)
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