We are in a new era of research transparency which requires advance planning for data sharing.
In this virtual session, participants will learn how to put together National Institutes of Health (NIH) data management & sharing (DMS) Plans, how to harmonize informed consent language with DMS Plans, and, if needed, how to translate the NIH DMS Plan to a ClinicalTrials.gov Individual Participant Data Plan.
Primary audience: Faculty and senior study team members from the University of Michigan or affiliated organizations who are involved in NIH-funded research. Part 1 of the workshop covers NIH grants; Part 2 covers those who work with human participants/patients; and for those who choose to stay, Part 3 covers content specific to clinical trials.
Registration is required.
*If you are interested in the training and cannot attend this workshop, please sign up to be notified about future workshops at the registration link.
**We aim to provide an outstanding experience for all attendees. If you require reasonable accommodations to attend, please get in touch with the organizers two weeks prior to the event at [email protected].