Join the UNC Office of Research Development and Innovate Carolina for an overview of the National Cancer Institute's 2026 SBIR/STTR programs and funding opportunities with Monique Pond, PhD, and Melissa Li, PhD, Program Directors from the SBIR Development Center at the NCI.
Whether you are considering commercialization of your research, planning a startup, or interested in translational funding, this session will provide valuable insights into NCI's small business funding programs, current priorities, and the application process.
This is the seventh session in the Systematic Review Summer Workshop Series offered by the UNC Health Sciences Library. This session will provide an overview of machine learning and automation tools available via the UNC Health Sciences Library for systematic reviews and other comprehensive literature searches. These tools help research teams save time by prioritizing literature search results and reducing the number of studies that must be screened manually for relevance.
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