INTERACTIVE RESPONSE TECHNOLOGY

Elevate the quality of all study types

Accelerate study design and ensure patients receive the right IP. Trust the cloud-based randomization and trial supply solution rated #1 in industry leadership.

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INTERACTIVE RESPONSE TECHNOLOGY

Advanced technology to optimize IP supply

Automation, predictive analytics, and remote monitoring enable sponsors to manage critical drug supply chains for complex study protocols.

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INTERACTIVE RESPONSE TECHNOLOGY

Deploy flexible, scalable IRT solutions

IQVIA IRT offers much more than innovative technology. Our experts initiate planning, build standard workflows, and ensure data integrity for all kinds of trials.
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Solutions IQVIA Technologies Patient Suite Interactive Response Technology
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Now Integrated into One Home for Sites!
We’re committed to reducing site burden from technology overload. Clinical research sites can now access IQVIA IRT from the One Home Single Sign-On Library.
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Adaptability to today’s study requirements

IQVIA IRT is a randomization and trial supply solution for your site-based or decentralized trial that supports today’s sophisticated trial protocols and ensures the right patient gets the right treatment at the right time:

Support sophisticated precision medicine studies


  • Reduced IP waste of expensive treatments through traceability
  • Support for temperature excursion management at the kit and shipment level
  • Custom-built modules are available for cell and gene therapy trials
  • Access to an experienced biostatistics team for designs ranging from simple to complex (blocked, adaptive, Bayesian, custom) randomization schemes
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Streamline site tasks with mobile technologies


  • Mobile IP integrates a user-friendly IRT mobile extension to improve risk-based management, returns, and re-supply
  • Turnkey workflows are available for direct-to-patient dispensation & confirmation
  • Automated forecasting and resupply management with predictive algorithms
  • Enhanced risk-based monitoring and audit trail analysis with electronic drug accountability, traceability, and returns management support
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Simplify integration with other clinical solutions


  • eConsent, eCOA, Site Portal, and decentralized trial platform integration
  • Augmented insights and reduced administrative burden through complimentary solutions and 400+ turnkey eClinical and drug supply integrations
  • Unified data delivery and management, reporting, and analytics
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Empower site staff with flexible, self-service capabilities


  • Self-service tools to manage SCRs and DCRs
  • Cohort management module for improved regulatory support of US FDA’s Project Optimus
  • Other important self-service modules including materials source update module, material management module, and dispensing module
  • Incorporation of sponsor standards (when applicable)

Accelerate time to deployment


  • Study Designer for collaborative and rapid prototyping to build, iterate, and finalize the study design
  • Advanced library of pre-built modules fast tracks platform design for simple to complex trials, which can be customized based on protocol adaptations
  • Cloud-based modular RTSM system built for configurability, rapid study start-up, and protocol amendments
Optimize IP supply chain management

Reduce time, effort, and cost in drug management by replacing siloed manual processes with the advanced supply and accountability capabilities of IQVIA IRT.

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Ensure delivery of high quality study data

IQVIA scientific and clinical experts understand what it takes to deploy sophisticated trials — from study design to delivery and change management.

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We chose IQVIA IRT as a preferred provider for many reasons. The user interface was strong and scored higher than other systems in having a portal that is easy to understand and offered a single enterprise login. [They] offer a robust audit functionality, a clear compliance trail, and a high level of customer service and support.

Associate Director, Information and Systems Strategy,

Leading Pharmaceutical Company

We have received positive feedback from end users and have recognized significant shipment cost savings compared to the previous period before implementation of SAVE. The journey has just started for us. The next step will be to leverage the tool expertise – with IQVIA support – into the entire drug supply manager community and include the tool in new trials.

Vendor Partnership & Governance team,

Leading Pharmaceutical Company

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ON DEMAND WEBINAR

Reducing risk in Cell & Gene Therapy trials with IRT

Learn about strategies for mitigating the complexities of Cell and Gene Therapy trials, while reducing risk and cost.

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Fact Sheet
IQVIA Interactive Response Technology
Blog
A New Approach to Meeting the Needs of Early Phase Trials with IRT
By: Nikki Pfammatter
Webinar
Ensuring a successful regulatory inspection with support from your IRT provider
Blog
Five Ways to Get Ready for Regulatory Inspections
By: Justine Koor
Article
Revolutionizing Personalized Medicine: How IRT Platforms are Transforming Cell and Gene Therapy Trials

Published on PharmaPhorum by Cara Woodruff, Director of Product Management, IQVIA IRT
Article
IRT: The Unsung Hero of Modern Trials

Published on HIT Consultant
Fact Sheet
Using IRT data to automate and optimize clinical supply

Save upwards of $20,000 a month through automated supply optimization
Blog
Three Tactics To Streamline Supply Chain Logistics
By: Maxime Schuchewytsch
Webinar
Case Study: Optimizing Clinical Supply Chain with Advanced Technology

Improve quality and sustainability while reducing cost and risk
Blog
Using tech enabled solutions to boost productivity and sustainability in clinical trials
By: Kevin Landells
Brochure
Medical Device Trial Integration

Learn more about how IRT improves quality and efficiencies in medical device trials
Article
Data-Driven Adaptive Trials: Enhancing Safety, Accelerating Progress and Boosting Economics Through Enhanced Insights

Published on Technology Networks Drug Discovery

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