University of Cincinnati Office of Research

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Results Guide for ClinicalTrials.gov (PDF)

Instructions on how to submit a protocol to ClinicalTrials.gov's Protocol Registration System(PRS); a web-based tool for submitting ClinicalTrials.gov. This document shows you how to use PRS for entering, modifying, and releasing study results.

Contact Office: HRPP

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FDA Training Material (PDF)

Clinical research overview for new investigators and information regarding the Investigational new drug/Investigational device (IND/IDE) assistance program.

Contact Office: HRPP

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Human Pluripotent Stem Cell (hPSC) Research (PDF)

This document provides information on Human Pluripotent Stem Cell
(hPSC) research, including an explanation of stem cells and their various forms, purposes, uses, involved ethics, and history of US federal regulation.

Contact Office: Biosafety

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Primer on Facilities and Administrative Costs (PDF)

This Primer is designed to provide background information about Facilities and Administrative (F&A) costs to members of the University of Cincinnati community. It begins with a brief history of F&A cost funding, then describes how F&A cost rates are calculated, defines the various cost components used to calculate an institutional rate, and explains how F&A cost recovery provides significant funding for the infrastructure and administrative activities necessary to carry out the University's research programs.

Contact Office: GCC

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UC Uniform Guidance Audit Report for FY19 (PDF)

Pursuant to Federal requirement, the University of Cincinnati has had an audit of its Federal awards performed in accordance with the requirements of Title 2 U.S. Code of Federal Regulations Part 200, Uniform Administrative Requirements, Cost Principles, and Audit Requirements for Federal Awards (Uniform Guidance).

Contact Office: SRS

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Occupational Health and Safety Information for Field Research (PDF)

An informational document that provides all of the regulatory required information for UC students that may be doing fieldwork on a limited basis (e.g. a class or two in the field). Students in this category must sign the document confirming that they understand the risks/regulations in field research. Students that do not handle vertebrate animals nor disturb the environment of the animals need not sign and return the form.

Contact Office: ACUP

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NIH Vertebrate Animal Section Check List (PDF)

This worksheet describes the information that must be included in applications submitted to NIH for activities involving the care and use of animals. It provides an overview of the requirements, a checklist for applicants and reviewers, detailed instructions, responsibilities of applicants, reviewers and NIH staff, and an example of an acceptable application.

Contact Office: SRS

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100 Protocol Submission and IACUC Review Policy (PDF)

There are several mechanisms for the review and approval of  submitted Animal Care and Use protocols and modifications to those protocols. All animal work for research, testing, or teaching must occur under an approved IACUC protocol. Protocols are approved for a maximum of 3 years. Prior to the 3-year expiration date, a triennial (de novo) review is required.

All documents requiring IACUC review must be submitted through the Research Administration Portal (RAP) system.

Contact Office: ACUP

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Authorized Medical Physicists Manual (PDF)

This manual is a compilation of relevant rules, regulations, policies, guidelines and procedures to be used a daily reference for the Authorized Medical Physicist (AMP) and is intended to provide instructions to AMPs and their RAM workers.

Contact Office: RadSafety

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