Appendix D: Pregnant Women and Neonates
This form should be used when pregnant women/ neonates are research subjects.
Appendix F: Waivers of Consent and Signatures or Alterations
This form is used when a waiver of informed consent, alteration of consent, or alteration or waiver of protected health information (PHI) is needed.
Appendix G: Exceptions from Informed Consent
This form is used when an exception from informed consent is needed.
Determination of Human Research Form
This form should be used when it is unclear whether the proposed activities require review by an Institutional Review Board (IRB).
F299: Request for UAHuman Research Site Authorization
Request for investigators who are not affiliated with the University of Arizona to access University resources to conduct human research.
IRB Renewal Guidance
Presentation outlining the processes and procedures for submitting a project renewal to the IRB. December 2015.
UAccess Research Proposal Provisioning Guide
Instructions for using the Access Provision Tool (APT) to to allow UAccess Research (UAR) campus units to distinguish between two department proposal approval roles in anticipation of upcoming proposal routing changes. December 2015.
IRB Amendment Guidance
Presentation outlining the processes and procedures for submitting a project amendment to the IRB. December 2015.
Statement of Compliance, UA Institutional Review Board, 2009
University of Arizona Institutional Review Board, Statement of Compliance, October 5, 2009. Signed by James L. Goodwin, Ph.D.
UAccess Research System Electronic Signature Policy
HSPP UAcess Research System Electronic Signature Policy letter, Mariette Marsh, October 10, 2014.