ART™ is a completely configurable solution for accountability and reconciliation that conforms to any protocol – giving you complete control over sites’ compliance with Good Clinical Practice (GCP).
ART™ is not just a tool for supply management and monitoring. It is vital for sites to achieve compliance, essential for CRAs to streamline their operations, and key for Clinical Operations to monitor, audit, and produce records.
ART™ (Accountability & Reconciliation Tracking)
ART™ (Accountability & Reconciliation Tracking) is a component of Almac’s IXRS®3 suite providing a digital chain of custody solution for supply accountability and reconciliation that includes the level of data integrity and traceability required by regulatory authorities.
ART™ combats common challenges of reconstructing a complete account of the chain of custody, which is often tedious, error-prone, costly and time consuming. ART addresses these factors and streamlines the process to improve site compliance and incomplete or inaccurate record – keeping across otherwise disparate clinical systems like IRT, EDC and paper forms.
ART™ utilises error-prevention workflows that eliminate data consolidation bottlenecks, and provides total control over and visibility into all supply chain events – transforming your chain of custody into a work of art.
ART™ Fact Sheet
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Our Favorite ART™ Features and Benefits
Streamlines the reconciliation process
Drastic reduction in billable hours of costly resources. Site monitors receives alerts for accountability discrepancies. Access to comprehensive reports to prepare timely remediation plans.
Traceability throughout the supply chain
The kits history and its details can be always accessed. Kit history information and status reports of the entire chain of custody of supplies are available in real-time
Speeds study close-out
IXRS®3 prohibits users from entering erroneous data which prevents discrepancies and greatly reduces time spent on drug reconciliation
Improves completeness and accuracy of accountability data
Documented returned investigational product (used, unused, missing, damaged)
Protects patient safety and reinforces compliance
ART captures both the drug assignment and details on the investigational product ensuring that what was dispensed to and consumed by.