Key features of IQVIA IRT
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Efficient study design and amendment
Simplified experience
Trial integrity and oversight
Reduce study cost and
IP waste
Intelligent integrations
and analytics
Efficient study design
and amendment
Advanced library of pre-built modules accelerates platform
design for simple to complex trials. Experienced designers
apply customization based on protocol or future adaptations.
Simplified experience
Intuitive design ensures data integrity and patient safety. Self-service tools improve trial efficiencies.
Trial integrity and oversight
Supporting protocol adherence, statistical integrity
and patient safety for 17+ years. Audit ready, real-time reports and innovative Machine Learning tools
improve quality and compliance.
Intelligent integrations and analytics
400+ existing drug supply and eClinical integrations. Feature-rich eCOA and eConsent integrations optimize trial quality and process.
Reduce study cost and IP waste
IQVIA IRT generates trials savings equal to or exceeding
the cost of IRT using advanced resupply optimization
technology (SAVE)
Cloud-based randomization and trial supply solution proven to reduce supply chain costs and improve study quality while accelerating study design, delivery and management
Simplified experience
Intuitive design ensures data integrity and patient safety. Self-service tools improve trial efficiencies.
Trial integrity and oversight
Supporting protocol adherence, statistical integrity and patient safety for 17+ years. Audit ready, real-time reports and innovative Machine Learning tools improve quality and compliance.
Intelligent integrations
and analytics
400+ existing drug supply and eClinical integrations. Feature-rich eCOA and eConsent integrations optimize trial quality and process.
Reduce study cost
and IP waste
IQVIA IRT generates trials savings equal to or exceeding the cost of IRT using advanced resupply optimization technology (SAVE)
