Key features of IQVIA IRT

Cloud-based randomization and trial supply solution proven to reduce supply chain costs and improve study quality while accelerating study design, delivery and management.

• Trial integrity and oversight
• Simplified experience
• Intelligent integrations and analytics
• Efficient study design and amendment
• Reduce study cost and IP waste

Adaptability, speed & insight

Learn more about IQVIA’s IRT - a randomization and trial supply solution for your site-based or decentralized trial that supports flexibility and optimization while ensuring the right patient gets the right treatment at the right time: Reduce trial supply costs

• Reduce costs with proprietary resupply algorithms and predictive, automated supply management that optimizes buffer stock automatically
• Improve decision making and study agility with forecasting for sites and depots built on real-time data and analytics Flexible randomization & treatment options
• Supports simple to complex randomization (blocked, adaptive, Bayesian, custom) options as well as novel trial designs
• Accelerates study start-up and protocol amendments with flexible, adaptable solutions and the right self-service tools
• Includes flexible at-home or on-site treatment dispensation options Temperature excursion management
• Enhances risk-based monitoring and audit trail analysis with electronic drug accountability, traceability and returns management support
• Supports temperature excursion management at the kit and shipment level Interoperability and connectivity
• Simplifies site and investigator experience and reduces data duplication with intelligent data integrations
• Enhances insights and reduces administrative burden through a suite of complimentary solutions and 400+ turn-key eClinical and drug supply integrations

Embrace the technology needed to improve the patient, site and sponsor experience

Patient

• Ensures the right drug gets to the right patient at the right time
• Technology speeds drug dispensation and reconciliation onsite and remotely
• Electronic drug accountability assists monitoring of patient compliance

Site

• User-friendly interface and shared data insights and reporting
• Integrated and shared workflows help sites perform faster transactions, leaving more time for patients
• Easy, turn-key integrations with 400+ trial support technologies and vendors, reduces administrative burden

Sponsor

• Self-service tools that facilitate trials activities, enhancing sponsor insights and improving communications with sites
• Rapid study design process reduces time to first-patient-in and improves quality with design prototyping and templates
• Intelligent tools and technology to optimize drug forecasting and resupply
• Data analysis and insights against key study metrics