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Home » OHRP Offers Tips on Reporting Clinical Trial Incidents
OHRP Offers Tips on Reporting Clinical Trial Incidents
September 11, 2014
Clinical trial staff should report serious or continuing noncompliance issues and unanticipated problems occurring at trial sites to HHS’ Office of Human Research Protections in no more than a month, says Kristina Borror, director of OHRP’s Division of Compliance Oversight.