In 2011, the University of Florida assembled a misconduct report about one of its ob-gyn researchers, identifying falsified data in a 2010 paper. But when an investigator at the U.S. Office of Research Integrity reviewed the report, something didn’t feel right.
“I reviewed the data, and I thought [UF] didn’t do their due diligence,” said Kristen Grace, then an ORI investigator, now heading up the compliance department of the Office of Clinical Research at the University of Pennsylvania. “Because the extent of the the falsification was so great.”
So the ORI asked the UF to re-open its investigation, expanding it to include previous years of work by Nasser Chegini, now retired. The institution also hired a new director of research compliance, who oversaw the second investigation. That report, completed in October 2013, was significantly more extensive — it documented intentional falsifications or fabrications in nine papers published between 2003-2008. (Through a public records request, we obtained a copy of this second report, which you can read in full here.) But last month, the ORI issued a finding of misconduct against Chegini that focused on only one paper; the agency said it chose to take a “targeted approach,” since eight of the nine papers had already been retracted.
The move has prompted a debate — while some argue it’s a pragmatic use of ORI’s limited resources, others (including Grace) are concerned:
Continue reading Recent finding of misconduct by federal U.S. agency sparks debate
