Clinical Research Coordinator Seminar Series
This series is designed for Clinical Research Professionals and others vested in the care of research participants. It provides opportunities for professional development as well as updates on Georgetown University policies, procedures and operations related to clinical research.
May 1: There will be a training on the use of 21CFR Part 11 DocuSign (research account) for use in FDA regulated studies.
All employees who need a research DocuSign account must attend training prior to receiving access. This will be the first opportunity for training.
Please share the meeting registration information with all those on your research teams needing access to a 21CFRPart11 research DocuSign account.
Register for the series (Zoom link will be added to your calendar automatically).
Coordinated by the Office of Human Subject Protections.