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As a global community, IQVIA continuously invests and commits to advancing human health.
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Regional Thought Leadership
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Choose a Region Contact Us
Explore IQVIA by region
As a global community, IQVIA continuously invests and commits to advancing human health.
Americas
Argentina Brazil Canada Central America and Caribbean Colombia Ecuador Mexico United States
Europe
Adriatic Nordics Belgium Poland Bulgaria Portugal Czech Republic Romania France Russia Germany Slovakia Greece Spain Hungary Switzerland Ireland Turkey Israel Ukraine Italy United Kingdom Netherlands
Asia & Oceania
Asia Pacific Australia & NZ China India Japan Korea Southeast Asia Sri Lanka
Middle East & Africa
Middle East and Africa
Regional Thought Leadership
US Insights
EMEA Thought Leadership
Asia Pacific Insights
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MAIN/Solutions
Solutions/
SOLUTIONS
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  • Real World Evidence
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LIFE SCIENCE SEGMENTS
HEALTHCARE SEGMENTS
THERAPEUTIC AREAS

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 Overview
Research & 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 OVERVIEW
Real 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 OVERVIEW
Commercialization 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 OVERVIEW
Safety & 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 OVERVIEW
Technology Quick Links
MAIN/Products
Products/
CLINICAL PRODUCTS
COMMERCIAL PRODUCTS
COMPLIANCE, SAFETY, REG PRODUCTS
REAL WORLD PRODUCTS

CASE STUDY

"Data in a Day

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MAIN/Insights
Insights/
BLOGS, WHITE PAPERS & CASE STUDIES

Explore our library of insights, thought leadership, and the latest topics & trends in healthcare.

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THE IQVIA INSTITUTE

An in-depth exploration of the global healthcare ecosystem with timely research, insightful analysis, and scientific expertise.

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INSTITUTE REPORT

"Global Trends in R&D 2025

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EMEA Insights

"IQVIA thought leadership with a focus on EMEA.

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WHITE PAPER

"DCTs Deliver Big ROI

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WHITE PAPER

"Capturing value at scale: The $4 billion RWE imperative

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MAIN/About
About/
FEATURED INNOVATIONS
  • IQVIA Connected Intelligence™
  • IQVIA Healthcare-grade AI®
  • Human Data Science Cloud
  • IQVIA Innovation Hub
  • Decentralized Trials
  • Patient Experience Solutions with Apple devices
WHO WE ARE
NEWS & RESOURCES

INVESTOR RELATIONS

"Visit our investor relations site for more information.

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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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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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IRT RESOURCES

Extend your understanding of IQVIA IRT here

Explore our library of IRT resources including thought leadership papers, on-demand webinars, case studies, and other valuable content.

Contact us
Solutions IQVIA Technologies Orchestrated Clinical Trials Patient Engagement Suite Interactive Response Technology IRT Resources

Whitepaper

Top Five Reasons You Need IRT Expertise (Not Just Software)

Explore how seeking an IRT specialist can improve planning, increase integration with other clinical systems, and mitigate study risks.

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Blog

Five Ways to Get Ready for Regulatory Inspections

Preparing for a regulatory inspection that includes your randomization and trial supply management (RTSM), commonly referred to as interactive response technology (IRT), during a clinical trial can be daunting, but there’s much that can be done to be ready for success. Read on to learn about the importance of clear roles, audit trails, data integrity, and training, and get recommendations to help you stay inspection ready.

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WEBINAR

Leveling up supply chain management to ensure accountability, sustainability & IP optimization

IQVIA experts discuss advancements in drug accountability delivered through IRT, which include managing site variances and ensuring a lean, sustainable supply chain.

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CASE STUDY

Using IRT data to automate and optimize clinical supply

Learn how SAVE reduces clinical team effort and reduces shipping and IP costs during studies.

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ARTICLE

IRT: The Unsung Hero of Modern Trials

Embracing IRT optimizes clinical trial operations, enhancing patient satisfaction, researcher efficiency, and sponsor results.

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FACT SHEET

IQVIA Integrated Complete Consent IRT eCOA

IQVIA’s approach to technology delivery provides exceptional value for sponsors and their patients in clinical trials.

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More IQVIA IRT Resources to Explore

Level Up Your Supply Chain Initiatives

Optimize technology to support faster, safer, and more reliable drug development.

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Medical Device Trial Integration

IQVIA IRT improves quality and efficiencies in medical device trials.

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Case Study: Optimizing Clinical Supply Chain with Advanced Technology

Enhance technology to ensure safety and accountability while minimizing costs and risks.

WATCH NOW
Beyond Integration: Flexible Orchestration of IRT and eCOA Solutions

Learn how this solution automates tasks, resolves redundant data entry, and enhances study communication for sites and sponsors.

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Fact sheets

Fact Sheet
IQVIA's Orchestrated IRT eCOA Solution
Fact Sheet
Electronic Drug Accountability and Returns Management
Fact Sheet
IQVIA Interactive Response Technology
Fact Sheet
Navigating The Use of Controlled Substances in Clinical Trials Using IRT
Case Study
Using IRT data to automate and optimize clinical supply
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CASE STUDIES

Case Study
Integration of IRT and eConsent with Unified Delivery Provides Robust Solutions to Clinical Trial Sponsor
Case Study
Intelligent IRT Design Process for COVID-19 Trials Accelerates Digital Enablement at Sites
Case Study
Pharma Sponsor Enlists Cenduit IRT to Rescue a Multi-Country, Multi-site Oncology Study
Case Study
Flexible Design for Novel Trials
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Thought Leadership

Explore insights from IQVIA IRT experts in clinical operations, therapeutic areas, and data management

ARTICLES

Article
Revolutionizing Personalized Medicine: How IRT Platforms are Transforming Cell and Gene Therapy Trials
Article
Data-Driven Adaptive Trials: Enhancing Safety, Accelerating Progress and Boosting Economics Through Enhanced Insights
Article
Reducing Clinical Trial Burden: How an Orchestrated IRT eCOA Solution Helps
Article
Using Tech-Enabled Solutions to Boost Productivity and Sustainability in Clinical Trials
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BLOGS

Blog
Using tech enabled solutions to boost productivity and sustainability in clinical trials
By: Kevin Landells
Blog
Three Tactics To Streamline Supply Chain Logistics
By: Maxime Schuchewytsch
Blog
Providing Drug Supply Support in Complex Environments through IRT
By: Stefan Duerr
Blog
Supply Chain Logistics Experts Share Best Practices
By: Maxime Schuchewytsch, Jeremy Star, Jonathan Walter, Stefan Duerr
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WEBINARS

Webinar
Ensuring a successful regulatory inspection with support from your IRT provider
March 18, 2025
Reducing the Impact of Macroeconomic Pressure on Trial Supply
IRT and Direct to Patient Trials

Related solutions

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.

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.

Complete Consent

Deliver eConsent to sites and study participants around the globe with confidence

Contact Us