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Oops! (I Did It Again): Issues with Human Subjects Research Data
August 31 @ 12:00 pm - 12:30 pm
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
HMS Research Staff, Faculty, Postdocs, Grad Students