IRT DELIVERY

Accelerate study design, delivery and management

IQVIA’s IRT experts partner with you to ensure protocol adherence, statistical integrity and patient safety for simple to complex trials.

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Solutions IQVIA Technologies Patient Suite Interactive Response Technology IRT Delivery

Establish strong partnerships with sponsors

IQVIA’s scientific, clinical, medical and operational experts initiate early planning, standardize workflows, and build intelligent integrations for successful execution for clinical trials.

Driving effective planning

Prepare for potential integration, supply chain, and data integrity issues to prevent costly retrofits and fixes
Plan for titrations, adaptive designs, open label studies, and stratification actors associated with complex trials
Establish study and supply chain health monitoring, enhance analytics, and control costs

Optimized supply chains

Ensure every patient receives medication on time while reducing over-supplying depots and sites
Provide ongoing vigilance, foresee potential risks, and take action when needed to maintain IP supply chain
Provide insights for baseline forecasting and ongoing modeling of the supply chain using real-world data
Expertise in depots, sites, regulations, and logistics to optimize IP supply chains in dozens of geographies

Data integrity and insights

Follow data sharing rules while integrating IQVIA IRT with other systems

Perform expert analysis of clinical and operational data to advise on risk mitigation and improve study health

Safeguard against unblinding risks through proper RTSM configuration and data-handling procedures

Experienced IQVIA IRT team

Experts at integrating IQVIA IRT with IQVIA eCOA and Complete Consent solutions
Dedicated IQVIA CORE team with delivery and project management leads, project managers, and engineers
Domain specialists in quality control, helpdesk, biostatistics, global project support, and other shared services
Effective communication and escalation pathways plus support for change management

Standards support drives faster deployment

IQVIA IRT offers an extensive library of 140+ pre-validated components—ready to use, easily configurable, and applied consistently across all studies

Minimal customization requires less effort
Pre-validated modules ensure compliance
Scalable for global trials of any size

400+ existing IQVIA IRT eClinical and drug supply integrations

IQVIA IRT has the flexibility to connect and share data with sponsor and CRO systems via simple file data transfers or API-driven integrations.

Self-service tools and modules

Empower sites with flexible tools that reduce system change requests and streamline change management for every trial type.

Site & patient updates

User creation & update, Site creation, Update site details & status, Subject demographic update, Subject visit update, Subject visit reset, Subject details update report, and Capping level/suspend update

Material & shipments

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

Supply strategy

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)

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