IRT Resources

  1. Beyond Integration: Flexible Orchestration Of IRT And eCOA Solutions 4/25/2023

    Consider how integrated response technologies and electronic clinical outcomes assessments can improve configurability, study start-up, and flexible mid-study changes.

  2. IRT? RTSM? What's The Difference? 10/4/2024

    What are the components of Randomization and Trial Supply Management (RTSM) and the critical role of RTSM and Interactive Response Technology (IRT) in clinical trials?

  3. 5 Ways To Get Ready For IRT Regulatory Inspections 7/31/2025

    Preparing for a regulatory inspection during a clinical trial can be daunting. Learn about the importance of clear roles, audit trails, data integrity, and training, and get recommendations to help.

  4. Unlocking The Value Of AI In IRT: Practical Perspectives From Vendors 12/5/2025

    AI can enhance IRT with predictive modeling and automation, but true success relies on high-quality data, compliance, and user trust. Learn practical strategies to boost efficiency.

  5. Benefit From Enhanced Power And Intelligence 8/14/2025

    Find a supply automation value engine with intelligent automation and algorithms to analyze drug supply data and automatically adjust delivery quantities to each site based on data available in IRT.

  6. Innovations In IRT 11/2/2023

    Review the latest innovative techniques employed by IQVIA IRT, including innovations in the design, delivery, conduct and monitoring of clinical trials.

  7. What To Look For In Your IRT/RTSM Solution For A Simpler Trial Execution 10/4/2024

    Which factors should you consider when selecting an IRT/RTSM vendor to ensure your trial's randomization and supply management processes are successfully executed?

  8. Impacting Sustainability Through Vendor Collaboration, Procurement 9/12/2024

    Guido D’Agostino, Head of Global Procurement at Chiesi, and Stefan Dürr, Senior Director of Product Management and Client Delivery at IQVIA IRT, delve into their achievements in sustainability.

  9. Efficiently Manage Clinical Data With Castor's EDC, CDMS 5/11/2023

    Effortlessly conduct multi-center clinical trials worldwide for drug development with Castor’s EDC and CDMS platforms, including eCOA, ePRO, EHR eSource, eConsent, and IRT modules.

  10. What Is The Suvoda Platform? 7/31/2025

    If you're ready to streamline your clinical trials and deliver better outcomes for all stakeholders, explore how the Suvoda Platform can transform your trial experience today.