Introducing TriNetX and Epic Cosmos
Peter Leese, MSPH, will introduce TriNetX and Epic Cosmos—the retrospective EHR data systems available at Carolina. Leese will also discuss the currently available published literature using data from these systems, as well as his perspective on using these systems to conduct high-quality, responsible research.
Speaker:
Peter Leese, MSPH
Program Director & Lead Scientist
TraCS Data Science Lab
Seminars in the NC TraCS Data Science Lab Seminar Series cover a range of topics related to health care data science, clinical data, data engineering, and working in these areas at UNC-Chapel Hill. These hybrid seminars are usually held monthly on the third Tuesday of each month from 12:30-1:30 p.m. in the NC TraCS suite (room 219) on the 2nd floor of Brinkhous-Bullitt or via Zoom.
This is the sixth session in the Systematic Review Summer Workshop Series offered by the UNC Health Sciences Library. This session will provide an overview of managing review data, including tips for data extraction and sharing data post-publication; guidance on structuring the review manuscript and including all required elements; and how to choose where to publish a review, based on the topic and methodology.
This workshop is being offered remotely via Zoom only. Registrants will receive a Zoom link; those on the waitlist will not receive a Zoom link unless they are bumped up to a registered spot.
ClinicalTrials.gov: Essentials for Academic Medical Centers
This virtual training is designed to help staff at academic medical centers meet the federal requirements for registering clinical studies and reporting results on ClinicalTrials.gov. Specialists from the Center for Drug Evaluation and Research (CDER), Center for Devices and Radiological Health (CDRH), Office of Clinical Policy (OCLP) and the Center for Biologics Evaluation and Research (CBER) within the U.S. Food and Drug Administration (FDA), and the National Library of Medicine (NLM) within the National Institutes of Health (NIH) will address frequently asked questions regarding regulatory obligations and the ClinicalTrials.gov Protocol Registration and Results System (PRS).
This training begins with a required, pre-recorded video that you can complete at your own pace prior to registering for the live panel session that best fits your schedule or area of interest. Upon completion of the pre-recorded training, we encourage you to submit questions for our expert panel to address during the live sessions. You can submit your questions by emailing
These sessions will help you and your team understand when and how to register and report clinical trial information to ClinicalTrials.gov and meet data transparency requirements. By completing the pre-recorded training and joining the live virtual panel, you will leave with practical information in order to share clinical trial information with the public accurately and on time.
On-Demand Video is available to watch on YouTube – Please View Before Registering.
There are three live panels offered. Register for the live panel session that best fits your schedule or area of interest.
- Option 1: Tuesday, July 14, 1-2 p.m. ET
- Option 2: Wednesday, July 22, 1-2 p.m. ET
- Option 3: Thursday, July 30, 1-2 p.m. ET