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The Following are forms to be used by the investigator when creating a
protocol for submission:
Preparatory to Research
Protocol Submission Checklist
Request for Scientific
Review
Waiver of Informed
Consent
Data Use
Agreement
Expedited Review
Submission
HIPAA Research
Authorization
(When you place the curser on a gray
area, in the follwoing form, please take note of instructions provided in the bottom right
corner, or you may press F1 and instructions will appear on the screen)
HIPAA Waiver Request for Corporate
Administrative Review
Specific Purpose Fund
Authorization
ISERB Informed Consent and
HIPAA Checklist
Instructions and a Template to be used when
creating the Informed Consent:
INSTRUCTIONS- Informed consent
template
Informed Consent
Template
To be used when the Investigator needs to Submit the Protocol for renewal
of approval:
Continuing Review
Application
Unaffiliated Investigator
Agreement
Guide to Scientific Submissions
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