The Drug Safety Triager is central to our success and is proven to deliver measurable efficiencies and cost savings whilst increasing productivity, compliance and quality in a fully validated and audit-ready package. It is a workflow application that has been designed from the ground up to allow review teams to focus on patient safety issues in the scientific literature and streamline the literature monitoring processes for ICSR, Aggregate Reports and Safety Signals.
The Drug Safety Triager provides complete management oversight, eliminates duplicated and inconsistent reference review and reduces the volume of literature that needs to be assessed by medics by 70-80%. After the review is complete, references containing patient safety issues are automatically output to case processing, medical writing and for signal evaluations.
Manages all incoming literature consistently, creating a systematic literature review process with added functionality all fully tested and compliant. For further information, please follow link above for White Paper.
Manages all incoming literature consistently, creating a systematic literature review process with an automatic audit trail
Easy to integrate
Integrates with existing safety databases and other workflow applications, such as full text and translation procurement, case management notification
Trusted and measurable
Trusted data from a high-quality scientific literature provider. Generate instant reports to measure compliance rates and instant KPI data
Streamlines the reference review process end-to-end for ICSR, aggregate reports and safety signals
Reduce risk in your literature monitoring process with a fully compliant, automated workflow