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Enabling Data-Driven Clinical Quality Assurance: Predicting Adverse Event Reporting in Clinical Trials Using Machine Learning.

Timothé MénardYves BarmazBjörn KoneswarakanthaRich BowlingLeszek Popko
Published in: Drug safety (2020)
The model has been deployed to evaluate safety reporting performance in a set of ongoing studies in the form of a QA/dashboard cockpit available to Roche Quality Program Leads. Applicability and production performance will be assessed over the next 12-24 months in which we will develop a validation strategy to fully integrate our model into Roche QA processes.
Keyphrases
  • clinical trial
  • adverse drug
  • emergency department
  • case control
  • open label
  • electronic health record
  • study protocol