The Office of Human Research Participant Protection/IRB has moved to a new off-campus location effective Monday, August 9, 2010.  The new location is:  1816 W. Lindsey, Suite 150  Norman, OK  73069.

Revised Forms Now Available!

Notice: Revised forms are now available from the links below and are marked with "*". Previous versions of these forms will be accepted through March 5, 2010. After that date, please use only the revised versions.

Application Forms

NOTE: Because changes will be made on a routine basis, forms must be downloaded prior to each use.  Hand-written copies of applications will not be accepted.  Original signatures must be on at least one copy of paperwork submitted to the IRB office. 

INITIAL APPLICATION FORMS

• Determination of Human Research Worksheet*
• IRB Application Form (All new study applications are to be submitted through the iRIS Study Submission System.)
  Please use this application for Full Board, Expedited and Exempt Studies.
• Certificate of Confidentiality (if applicable)

• Appendix A -- Protocol Description (Revised 02/24/2012)
• Appendix B -- Student as Principal Investigator
• Appendix C -- International Research Review Form
• New Research Project Application Supplement for DoD Research

CONSENT FORM DOCUMENTS

• Informed Consent Template (Revised 02-24-2012)
• Informed Consent Form - Required Elements
  Information required by Federal Law to be provided in the Informed Consent Form.
• Information Sheet for Consent to Participate in a Research Study (Revised 11-01-2011)
• Assent Template (Revised 11-01-2011)
• Debriefing Template
• Translator Statement Template

ANNUAL REVIEW FORM/PROGRESS REPORT

• Continuing Review Form

  This form is for annual continuing review purposes.

MODIFICATION FORM

• Modification Form
  Form for all amendments and revisions.

PROTOCOL DEVIATION FORM

• Protocol Deviation Form

CONFLICT OF INTEREST

• Conflict of Interest Disclosure Form
• Examples of Conflicts of Interest

UNANTICIPATED PROBLEM

• Unanticipated Problem*
  Form for reporting all unanticipated problems (ex: subject recruitment issues, compensation to participants, inclusion/exclusion criteria, costs to participants, informed consent issues, documentation of informed consent, privacy or confidentiality protections, vulnerable subject protections, etc.).

HIPAA FORMS

• Authorization to Use or Disclose Protected Health Information for Research
• Request For Waiver Of Authorization