A Simple Hack To Help CRAs Process or Verify Adverse Events In Clinical Research Quicker

Every medication that a patient takes during a clinical trial should be carefully documented by sites to ensure that any potential drug interactions are captured. CRAs that review either source documents or EDC entries for concomitant medications (Con-meds) are expected to verify that the site is accurately capturing these medications. This can typically be done by making sure that new Con-meds correlate with a patient’s Adverse Event (AE) or medical history.