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".
A ribbon-cutting ceremony to celebrate the opening of the Wisconsin Alzheimer’s Disease Research Center's Community Data Collection Site at the UW South Madison Partnership office.
Join us for the rolls, strolls, walks and more and stay for the music, food, raffle, games, fun and more.
OutReach LGBTQ+ Community Center will be hosting its 5th Annual Magic Pride Festival in Madison's Warner Park!
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.
This event is a great way to learn more about approved research concepts and connect with other researchers within the SMPH community.
This webinar will discuss the best practices in various areas of clinical research management of investigator-initiated trials (IITs) and detail how to navigate common challenges.
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 speaker will be Dr. Quincy Byrdsong, a nationally recognized speaker in the areas of dynamic education programs and curricula for research administration, responsible conduct of research, and human subjects protections.
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.
This presentation aims to inform research staff of the different factors that influence the IRB review of multi-site projects and trigger the need for reliance agreements.
