"We strive to help improve outcomes and create a healthier, more sustainable world for people everywhere.
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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
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
Elevate commercial models with precision and speed using AI-driven analytics and technology that illuminate hidden insights in data.
COMMERCIALIZATION OVERVIEW
Orchestrate your success across the complete compliance lifecycle with best-in-class services and solutions for safety, regulatory, quality and medical information.
COMPLIANCE OVERVIEW
When your destination is a healthier world, making intelligent connections between data, technology, and services is your roadmap.
TECHNOLOGIES OVERVIEWExplore our library of insights, thought leadership, and the latest topics & trends in healthcare.
DISCOVER INSIGHTSAn in-depth exploration of the global healthcare ecosystem with timely research, insightful analysis, and scientific expertise.
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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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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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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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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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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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Empowering patients to personalize their healthcare and connecting them to caregivers has the potential to change the care delivery paradigm.
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"At IQVIA your potential has no limits. We thrive on bold ideas and fearless innovation. Join us in reimagining what’s possible.
VIEW ROLESProviding you with regulatory strategy, labeling, publishing, and intelligence solutions supported by our global expertise, data and technology, from early drug development through submissions and post-registration.
Navigate changing regulatory demands with greater accuracy, agility and efficiency. Let us help you where you need it most. Our 3,300+ experienced regulatory affairs professionals stand ready to assist anywhere across the product lifecycle, in more than 65 global locations.
Our Regulatory Affairs professionals help biopharma and MedTech companies handle regulatory workflows more flexibly, productively, and efficiently. From strategic regulatory advice to regulatory maintenance and lifecycle management, we’ve got you covered from early drug development through submissions and post-registration. IQVIA’s regulatory strategy, labeling, publishing, and intelligence solutions provide:
Advances in artificial intelligence (AI) and machine learning (ML) have long helped other industries. Now it is happening in healthcare. By leveraging deep scientific and health system expertise, IQVIA provides technology-enabled solutions, from site selection through post-launch safety, and can also help you respond in near real-time to regulators as well as payer and provider demands for evidence. That’s the power of analytics and data structured for the distinct needs of your organization.
IQVIA RIM Smart. Intelligence, automation and integration.
Boost your regulatory productivity.
Automate and standardize your regulatory management, from correspondence and commitments to registration and tracking.
