Course Objective

What happens when something goes wrong with human subjects research data? Is it an IRB or regulatory issue? What corrective actions need to happen, if any? When do I have to notify my participants?

Expert(s): Kim Serpico, MEd, CIP, Associate Director of IRB Operations, Office of Regulatory Affairs and Research Compliance, Harvard T.H. Chan School of Public Health

Target Audience

HMS Research Staff, Faculty, Postdocs, Grad Students