| Protocol
(IRB-1) Instructions
Please type
or the application will be returned to you.
- Do not attach
abstracts, dissertations, etc. to this application. All information
pertaining to this study must be contained in the body of this
application, however, reference materials or supporting literature
may be attached.
- Please provide
information as requested. If any specific section is not applicable
to the study being submitted, please indicate with NA rather than
leaving it blank.
- Page numbers
should appear on every page of the protocol application.
- If multiple
consent forms are to be used for a single study, they should be
identified by subject population or experimental condition.
- Page numbers
should appear on every page of the consent form. Each consent
form should begin with number 1.
- Copies of
all questionnaires/survey instruments used in the study must be
submitted with this application.
- Copies of
all consent forms, questionnaires and other study-related materials
that have been translated into a foreign language must be submitted
with this application.
- Copies of
all advertisements/recruitment materials must be submitted with
this application, if available. If they have not been developed
at the time of submission, they must be submitted for review as
an amendment before being utilized.
- One copy
of each applicable grant application must be submitted with this
application.
- Download
& Complete the Protocol (IRB-1) form.
For Expedited
Review:
When the protocol is completed, submit one (1) original and one
(1) copy of the full IRB Application (note: only one copy of the
grant application is necessary).
For Full
Board Review:
When the protocol is completed, submit one (1) original and fifteen
(15) copies of the full IRB Application (note: only one copy of
the grant application is necessary).
Please forward
all materials to:
The Office of Research Compliance
Whetten Graduate Center, # 214
438 Whitney Road Ext. Unit 1246
Storrs, CT 06269-1246
Please direct
any questions, concerns, or comments to:
The Office of Research Compliance
860-486-8802
irb@gris.grad.uconn.edu
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