Power your decentralized trial with an agile randomization and trial supply management solution that supports supply flexibility and optimization as well as adaptable direct to patient options.
IQVIA’s scientific, clinical, medical and operational experts initiate early planning, standardize workflows, and build intelligent integrations for successful execution for clinical trials.
IQVIA IRT offers an extensive library of 140+ pre-validated components—ready to use, easily configurable, and applied consistently across all studies
IQVIA IRT has the flexibility to connect and share data with sponsor and CRO systems via simple file data transfers or API-driven integrations.
Empower sites with flexible tools that reduce system change requests and streamline change management for every trial type.
Update material status at site or depot, Stop or resume shipments, Raise manual shipments to depot or site, Cancel shipments to depot or site, Update do not ship or start replacement parameters, Quickly block material with quality or safety issues, Depot & site quarantine release
Create a new custom strategy (Set Forecast window and initial shipment setting), Update site or group parameters for existing strategy (Unblinded resupply strategy update), Update site assigned strategy (e.g., low to high)
Power your decentralized trial with an agile randomization and trial supply management solution that supports supply flexibility and optimization as well as adaptable direct to patient options.
Improve study quality, accelerate decision making and reduce site and sponsor burden by harnessing the power of IQVIA’s integrated Interactive Response Technology (IRT) and electronic Clinical Outcome Assessment (eCOA) solution.
Technology informed by unparalleled Decentralized Trials (DCT) operational experience and delivered at global scale.