Investigator Manual Index
What is the purpose of this manual?
What is the Human Research Protection Plan?
What training do investigators and study staff need to conduct Human Research?
How to submit new non-exempt Human Research to the IRB
How to complete "FORM: Initial Application for Human Research"
How to write a Protocol Summary and/or Detailed Protocol
What financial interests have to be reported to the IRB?
How to create a consent/assent document
How does the IRB decide whether to approve Human Research?
What will happen after IRB review?
What are the Investigator's obligations after IRB approval?
How to submit continuing review
How to get help for an IRB submission
Are there any services available to assist investigators with ensuring regulatory compliance?
How long should records be kept?
How to get additional information and answers to questions
If you have any questions please contact Leslie Howes at 617-384-5487 or Julie Kaberry at 617-384-8547.
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For any other questions, please contact OHRA.