Human Subjects Applications & Forms

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When preparing submissions to Research Compliance Services (RCS), please use the most current version of the materials below to avoid delay in the IRB review process. Version dates are noted in the footer within the document. As a courtesy, prior versions will be accepted up to 90 days after a new version is posted.
Forms and
Applications
Use/Description Form/Templates Guidance

Initial Review
Application

  • Submit to request Initial IRB Review (i.e., Expedited or Full review)

Exempt Review Application and Worksheets

  • For self-assessment and screening for exemption eligibility.
  • Submit to request an Initial Exempt Determination.
  • Submit to request review of proposed changes to a previously determined exempt protocol.

Amendment Review
Application

  • Submit to request a change in a previously approved Exempt, Expedited, or Full Review protocol.
  • Submit to request a protocol be assessed for transition to the 2018 revised Common Rule.

Continuing Review
Application

  • Submit 45 days in advance of protocol expiration to request continuation of previously approved protocols that were determined to require continuing review (i.e., Full Review and some Expedited).

Progress Report/
Study Closure
Application

  • Submit at least 45-days in advance of a protocol expiration to:
    • Request a previously approved protocol be closed as human subject research activities are complete.
    • Request an extended project period for a protocol determined to be Exempt. 
    • Request an extended project period for an Expedited protocol that was determined to not require continuing review.
  • NOTE: Expedited protocol that require continuing review must use the Continuing Review Application Form.

Approval in Principle
Application

  • The AIP application and approval allows UO Sponsored Project Services (SPS) to release funds associated with preliminary phases of research that are preparatory to planned human subject research activities.  Submit this application to facilitate review for these conditions.

Approval-In-Principle
Guidance

Event Report Form

  • Submit this form to report to RCS and the IRB any unanticipated problems or events (e.g., protocol deviations, non-compliance, participant complaints, etc.)

Human Subjects 
Research Determination Form

  • Use this form to determine if your project meets the definition of human subject research and requires submission of a protocol.
  • Submit this form if you need formal documentation that your study does not require further review OR if you are uncertain if your project requires further review.

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Application Attachments Use/Description Forms/Templates Guidance

Funding and
Sponsorship Form

  • Include this form with an initial review or exemption application if your study is funded.
  • Include with an amendment application when funding has changed or is being added.

Research Personnel
Form

  • Include with all initial, exempt determination, and continuing review applications.
  • Include with amendments when changes to personnel are proposed.
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Conflict of Interest (COI) Form

  • This attachment must be completed individually by the Principal Investigator (PI), Faculty Advisor, and each person having responsibility for the design, conduct, and/or reporting of the research.
  • The PI must submit this form only for:
    • New research personnel who have identified a real, perceived, or potential conflict of interest on their form. Submit the form(s) with either the Initial Review application or the Amendment Application.
    • Existing personnel who have identified a change to a real, perceived, or potential conflict of interest on their form. Submit the form(s) with an Amendment Application.
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IRB Authorization Agreement (IAA) Request Form

  • Include with initial, exempt determination, and amendment applications when requesting IRB oversight be deferred to either UO or a collaborating institution.

Individual Investigator Agreement (IIA) Form

  • Include with initial, exempt determination, and amendment applications when a member of the research team is independent and unaffiliated with an institution.

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Protocol Materials
and Guidance
Use/Description Forms/Templates Guidance

Guidance Library

  • Guidance Library provides additional topical guidance.
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Research Plan

  • The Research Plan is a narrative of the study and is a living document to be maintained over the life of the protocol. A Research Plan is required for every protocol submitted for IRB review.

Appendix A - Drugs & other Substances

  • Use this as an appendix to the Research Plan to provide information to the IRB when your study involves the use of drugs and other substances.
  • Provide an appendix for each drug or substance in your research.

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Appendix B - Investigational Device

  • Use this as an appendix to the Research Plan to provide information to the IRB when requesting a Nonsignificant Risk (NSR) device determination for an Investigational Device (IDE).
  • Provide an appendix for each investigational device in your research.

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Appendix C - Ionizing Radiation

  • Use this as an appendix to the Research Plan to provide information to the IRB when your research involves the use of ionizing radiation.

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Appendix D - HIPAA/ Use of Protected Health Information (PHI)

  • Use this as an appendix to your Research Plan when your research involves use of Protected Health Information under the HIPAA Privacy Law.

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Appendix E - Research Involving Genetic Information/Tests

  • Use this as an appendix to your Research Plan to provide information to the IRB when your research involves genetic information/tests.
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Informed Consent 
and Assent
Use/Description Forms/Templates Guidance

Informed Consent
Form

  • Use the guidance and template form to develop an adult consent form.
  • The guidance incorporates the regulatory requirements for informed consent and may be modified to meet the needs of the research design or participant population.  

Assent Form/Script

Coming Soon! Coming Soon! n/a

Oral Consent Script

Coming Soon! Coming Soon! n/a

HIPAA Authorization
Form

  • Use this template form to develop a HIPAA Authorization for use or disclosure of protected health information.

Release Form for Translators and Transcribers

  • Use this template form for translator/transcriber agreement of confidentiality provisions
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