Complete Consent
Deliver eConsent to sites and study participants around the globe with confidence
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Americas
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Asia & Oceania
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EMEA Thought Leadership
Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
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Middle East & Africa
EMEA Thought Leadership
Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
Learn more
Regions
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Americas
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Asia & Oceania
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Europe
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Middle East & Africa
SOLUTIONS
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Research & Development
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Real World Evidence
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Technologies
LIFE SCIENCE SEGMENTS
HEALTHCARE SEGMENTS
- Information Partner Services
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THERAPEUTIC AREAS
- Cardiovascular
- Cell and Gene Therapy
- Central Nervous System
- GI & Hepatology
- Infectious Diseases and Vaccines
- Oncology & Hematology
- Pediatrics
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Impacting People's Lives
"We strive to help improve outcomes and create a healthier, more sustainable world for people everywhere.
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Harness the power to transform clinical development
Reimagine clinical development by intelligently connecting data, technology, and analytics to optimize your trials. The result? Faster decision making and reduced risk so you can deliver life-changing therapies faster.
Research & Development OverviewResearch & Development Quick Links
Real World Evidence. Real Confidence. Real Results.
Generate and disseminate evidence that answers crucial clinical, regulatory and commercial questions, enabling you to drive smarter decisions and meet your stakeholder needs with confidence.
REAL WORLD EVIDENCE OVERVIEWReal World Evidence Quick Links
See markets more clearly. Opportunities more often.
Elevate commercial models with precision and speed using AI-driven analytics and technology that illuminate hidden insights in data.
COMMERCIALIZATION OVERVIEWCommercialization Quick Links
Service driven. Tech-enabled. Integrated compliance.
Orchestrate your success across the complete compliance lifecycle with best-in-class services and solutions for safety, regulatory, quality and medical information.
COMPLIANCE OVERVIEWSafety & Regulatory Compliance Quick Links
Intelligence that transforms life sciences end-to-end.
When your destination is a healthier world, making intelligent connections between data, technology, and services is your roadmap.
TECHNOLOGIES OVERVIEWTechnology Quick Links
CLINICAL PRODUCTS
COMMERCIAL PRODUCTS
COMPLIANCE, SAFETY, REG PRODUCTS
BLOGS, WHITE PAPERS & CASE STUDIES
Explore our library of insights, thought leadership, and the latest topics & trends in healthcare.
DISCOVER INSIGHTSTHE IQVIA INSTITUTE
An in-depth exploration of the global healthcare ecosystem with timely research, insightful analysis, and scientific expertise.
SEE LATEST REPORTSFEATURED INNOVATIONS
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IQVIA Connected Intelligence™
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IQVIA Healthcare-grade AI®
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IQVIA AI Assistant
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Human Data Science Cloud
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IQVIA Innovation Hub
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Decentralized Trials
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Patient Experience Solutions with Apple devices
WHO WE ARE
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NEWS & RESOURCES
Unlock your potential to drive healthcare forward
By making intelligent connections between your needs, our capabilities, and the healthcare ecosystem, we can help you be more agile, accelerate results, and improve patient outcomes.
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IQVIA AI is Healthcare-grade AI
Building on a rich history of developing AI for healthcare, IQVIA AI connects the right data, technology, and expertise to address the unique needs of healthcare. It's what we call Healthcare-grade AI.
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Meet the IQVIA AI Assistant
Your new expert analyst is here. Be at the forefront of data-driven decision-making with a new generative AI tool that enables you to interact with our products and solutions like never before. Get results you can trust, faster.
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Your healthcare data deserves more than just a cloud.
The IQVIA Human Data Science Cloud is our unique capability designed to enable healthcare-grade analytics, tools, and data management solutions to deliver fit-for-purpose global data at scale.
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Innovations make an impact when bold ideas meet powerful partnerships
The IQVIA Innovation Hub connects start-ups with the extensive IQVIA network of assets, resources, clients, and partners. Together, we can help lead the future of healthcare with the extensive IQVIA network of assets, resources, clients, and partners.
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Proven, faster DCT solutions
IQVIA Decentralized Trials deliver purpose-built clinical services and technologies that engage the right patients wherever they are. Our hybrid and fully virtual solutions have been used more than any others.
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IQVIA Patient Experience Solutions with Apple devices
Empowering patients to personalize their healthcare and connecting them to caregivers has the potential to change the care delivery paradigm.
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WE'RE HIRING
"At IQVIA your potential has no limits. We thrive on bold ideas and fearless innovation. Join us in reimagining what’s possible.
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ON DEMAND WEBINAR
Ensure a successful regulatory inspection
Watch on demand as IQVIA IRT discusses preparing for regulatory inspections. Learn about the latest trends and explore five key areas of regulatory focus to stay ahead in the regulatory landscape.
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
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
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
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.
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.
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.
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.
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.
Learn More
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
Case Study
Using IRT data to automate and optimize clinical supply
Save upwards of $20,000 a month through automated supply optimization
Webinar
Case Study: Optimizing Clinical Supply Chain with Advanced Technology
Improve quality and sustainability while reducing cost and risk
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
Article
Level Up Your Supply Chain Initiatives
By Maxime Schuchewytsch, Associate Director of Product Management, Cenduit IRT, an IQVIA Business
Article
Reducing Clinical Trial Burden: How an Orchestrated IRT eCOA Solution Helps
Published on MedHealth Outlook
Fact Sheet
IQVIA Integrated Complete Consent IRT eCOA
Interoperable technology that improves data quality and usability while optimizing trial conduct
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IRT eCOA
Improve study quality, accelerate decision making and reduce site and sponsor burden by harnessing the power of IQVIA’s integrated Interactive Response Technology (IRT) and electronic Clinical Outcome Assessment (eCOA) solution.
eCOA
Fast, flexible and proven, IQVIA’s industry-leading electronic clinical outcome assessment (eCOA) platform ramps up efficiencies, delivers real-time data, and sharpens insights through best-in-class technology and a better patient experience.