Template worksheet and sample budget for industry-sponsored clinical trials. Useful for budgeting clinical trials/studies.
The Schema Review Memo, along with the reviewed protocol schema, is required prior to Banner and UA IRB review. The Memo provides documentation of the schema review process by the Principal Investigator and the Epic Charge Validator. If there is no Charge Validator because the study will not utilize Banner services, the Study Coordinator information should be provided instead. A blank Schema Review Memo is provided in this link along with three examples of reviewed protocol schemas.
Retrospective Chart Review projects using HSPP Form F203 do not require submission of this document.
Instructions:
1) Complete the Memo, including the required signatures.
2) Follow the instructions on the Memo to review the Protocol Schema, Schedule of Events, or Calendar of Events. If a schema is not included in your protocol, create a list of the research events in a Word document. Include a statement, "All circled protocol events are research-related and not part of routine care."
3) Circle services that are research-related and not considered routine care (standard of care).
4) The PI and the Epic Charge Validator must print their names, sign, and date the reviewed Schema or Calendar of Events.
4) Upload the Memo and reviewed Schema to the online submission form.
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.
Outlines the position of the University of Arizona on Epic Electronic Health Record (EHR) compliance with FDA 21 CFR 11 requirements.
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.