UW Clinical Trials Institute

Engage with leaders within the UW clinical research community at this open Q+A ‘Research Forum’. This is an opportunity to ask questions about clinical research-related topics such as the IRB, informatics, and clinical trials.

Learn more about the Industry-sponsored Clinical Trials Budget Template, its supporting documentation, and how to access/use it in OnCore. Also, hear about lessons learned from the 8-month pilot and suggestions and best practices for using the template. The Budget Template will launch July 1 and will be required for industry sponsored clinical trials at UW moving forward.

Learn from the IRB what types of events constitute potential unanticipated problems or noncompliance that require report to the IRB as a "reportable event".

Learn about clinical research that is focused on the safety and novel therapeutic use of psychoactive medications, including psilocybin for depression and substance use disorder and MDMA for PTSD.

Engage with leaders within the UW clinical research community at this open Q+A ‘Research Forum’. This is an opportunity to ask questions about clinical research-related topics such as the IRB, informatics, and clinical trials.

The UW ClinicalTrials.gov Service will review the requirements around whether summary results are due to ClinicalTrials.gov, the data that are expected to be reported, and a typical timeline for the results reporting process.

Dr. Kind is an international leader in the fields of social determinants of health and mechanistic health disparities research, leading the team that developed the Neighborhood Atlas, a free first-of-its-kind data democratization tool that quantifies socioeconomic disadvantage for every neighborhood in the US including Puerto Rico.

This session will give an overview of the new Participant Payments system being implemented at UW-Madison to pay research participants for stipends and travel in a single system.