Research With Humans

Institutional Review Board (IRB)

 Office of Human Research Protection Information

• Research Involving Children
• Policy and Guidance
• DHHS Home Page

 

 PI Responsibilities 

All PIs and Co-Investigators must complete the following on-line

training course before any IRB approvals

http://cme.cancer.gov/clinicaltrials/learning/humanparticipant-protections.asp

IRB Handbook

  Forms:

• IRB Modification Request Form
• IRB Adverse Event Report Form
• IRB Continuing Review Form
• IRB Dean-Chair Approval of Study Form
• IRB Discontinuance of Study Form
• IRB Exempt Research Application Form
• IRB Expedited Research Application Form
• IRB Full Board Review Application Form
• IRB Informed Consent Form
• IRB Member Agreement Form