IRB Worksheet for Initial Review
Protocol ID
*
Protocol Title
*
Reviewer Name
*
First Name
Last Name
E-mail
*
To approve research the following minimum criteria must be present:
Does the protocol have scientific merit?
*
Yes
No
If no, why not?
Is the protocol written in order to minimize risk to participants?
*
Yes
No
If no, why not?
Is the selection of participants equitable (fair and reasonable)?
*
Yes
No
If no, why not?
Are the participants’ risks balanced by the potential benefits of the research?
*
Yes
No
If no, why not?
Are the rights and welfare of research participants adequately protected?
*
Yes
No
If no, why not?
Are there adequate plans to protect the privacy and confidentiality of participants and their data?
*
Yes
No
If no, why not?
Is the informed consent process adequate?
*
Yes
No
N/A
If no, why not?
If there is risk to the participants, does the protocol make adequate provision for monitoring the study and the data collected so that risks to participants are minimized?
*
Yes
No
N/A
If no, why not?
If vulnerable groups are enrolled, are there adequate safeguards in the study design and consent process to protect these persons from undue influence and/or coercion?
*
Yes
No
N/A
If no, why not?
Are the protocol and IRB application congruent and are they both reflected accurately in the informed consent form?
*
Yes
No
N/A
If no, why not?
Does the Principal Investigator have qualifications and experience to adequately perform the research proposed?
*
Yes
No
If no, why not?
Comments
Recommendations
*
Approve
Approve pending revisions
Table
Disapprove
Continuing Review Recommendation
Annual
Less than one year
Reviewer Signature
Today's Date
*
/
Month
/
Day
Year
Date
SUBMIT
Should be Empty: