Description
This webinar covers a brief overview of the regulations, important timelines to follow, agency-specific variances, and a range of compliance mechanisms. It also covers the specific steps a major university took to build a successful compliance program to assist investigators. It concludes with information on how to connect with a national taskforce, which provides resources that help organizations become more compliant.
Audience
Clinical Researchers, Clinical Research Coordinators, Investigators, Sponsors
Meet the Presenter
Anthony Keyes, MBA, PMP – Johns Hopkins University
Anthony Keyes is a Program Manager with 15 years’ experience in clinical trial management. He directs the Johns Hopkins ClinicalTrials.gov Program and co-chairs the Clinical Trial Registration and Results Reporting Taskforce. He received his MBA from Johns Hopkins University, a BS from the University of Maryland, and is a certified Project Management Professional.