The UC Davis Clinical Trials Office provides centralized support to clinical trials. Our comprehensive expertise includes study management, budgets, coverage analysis , IRB, FDA and others. We collaborate with Compliance and Contracts in areas of budgets for industry-sponsored studies, HIPAA and Clinical Research Billing.

In 2016-2017 the CTO will hold office hours, open to all investigators and staff at UC Davis, to bring forth immediate questions that arise during the performance of the study. Please note that these hours are for consultation and Q&A purposes only. Should more work be required, you will be asked to apply for resource use though CTSC.

In addition, the CTO will have hands-on stations to enable introductions to CPR, EKG and manual blood pressure. No certificates will be issued for attending these stations.

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