The purpose of the Clinical Research Guidebook is to provide a road map to navigate the processes and procedures for conducting clinical research at UC Davis. The Guidebook can also serve as reference for investigators and site staff as to the federal regulations governing clinical research in the United States.

The 2015-2016 Edition of the Guidebook is divided into twelve activities organized to help the investigators and their staff navigate through the various requirements of clinical research at UC Davis. The Guidebook is not meant to be all inclusive; more help is available from the UC Davis Clinical and Translational Science Center, the UC Davis IRB, Health System Compliance and Health System Contracts – Clinical Trials Contracts

This Guidebook references materials from other sources with references cited whenever possible. Every effort was made to ensure the information is accurate as of the date of the publication.

Pre-order your own spiral-bound paper copy of the Guidebook by filling out information below.

We will be ordering bulk printing based on the number of orders.

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