Webinar: Investigator-Initiated Trial Tips and Tricks
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.
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.
This event is a great way to connect and communicate with other members of the SMPH community and learn more about the research surrounding diabetes.
All are invited to register to attend this free community educational event that will offer news about cutting-edge research in Alzheimer's disease and provide information to help people improve brain health and live healthier lives.
By walking, running, or biking, you can show your support for cancer research and the development of new treatments.
Join us for an informal, drop-in breakfast in the Health Sciences Learning Center (HSLC) Atrium.
The Annual Colloquium will showcase the latest research and resources on positive aging, with Speakers, a Poster Session, and a Health & Resource Fair.
The annual Black Women's Wellness Day will feature a powerful mix of Information, Inspiration, and Empowerment.
This presentation will provide an overview of the policy, the process for creating a DMS plan, and what to consider for IRB applications and informed consent documents.