Events

Oops! (I Did It Again): Issues with Human Subjects Research Data

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. […]