Lists typical pharmacy fees associated with clinical trials/studies, and includes contact information for studies at various UAMC locations.
A list of common personnel costs for clinical studies/trials. Useful for estimating time and effort on specific tasks when constructing a clinical trial/study budget.
This form collects information that allows the Bioinstrumentation Subcommittee to evaluate a request for funding related to a new core/shared research service. Please also review the Bioinstrumentation Guidelines and submit a corresponding Research Equipment Funding Request Form.
A template letter claiming exemption from the Arizona Board of Regents Intellectual Property Policy, based on meeting the criteria outlined here. Relevant to the clinical research contract review process.
This form is required as part of the clinical research contract review process when the contract type is a Material Transfer Agreement (MTA).
Per NIH and NSF restrictions (and certain other funding agencies), postdoctoral trainees receiving support directly from an Individual or institutional training grant must forfeit their employer-employee relationship with the UArizona. This memo outlines financial support for healthcare benefits purchased by a postdoctoral fellow receiving a training award up to 25% of the total cost. Post-doctoral training grant (T32) PIs and mentors trainees on post-doctoral F-awards should contac Jenny Hoit (hoit@arizona.edu) to request this support from RII.
This policy is intended to protect medical student confidentiality and provides restrictions on requests for and use of College of Medicine – Tucson (COM-T) undergraduate Medical Education Data for research and program improvement purposes. Data requests must be submitted to and approved by the Accreditation & Analytics Office. Medical Education Data must be used in a manner that protects student confidentiality.
This document lists the criteria which must be met to qualify for an exemption from the Arizona Board of Regents Intellectual Property Policy. Relevant to the clinical research contract review process.
A list of invoiceable items for clinical trials/studies. Useful for clinical study budgeting.
A policy memo stating the circumstances in which indirect cost (F&A) waivers may be granted, and the process for requesting such a waiver.