Detecting, Handling, And Reporting Data Falsification, Misconduct, And/Or Suspected Fraud

Clinical research associates (CRAs) must be aware of the many signs of possible fraud or fabricated data occurring at a clinical trial site. Whether indications of fraud appear as missing documentation, altered numbers, signatures that don’t match, or unavailable medical records, CRAs need to look for signs and understand the proper protocol to handle and report the misconduct during each monitoring visit.