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 IRB - Human Subjects in Research

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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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