Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
Learn more
Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
Learn more
Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
Learn more
Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
Learn more
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 and quality.
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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Artificial intelligence is accelerating opportunities. Realizing the benefits for healthcare requires the right expertise. Together, we can solve the problems of today, and drive the breakthroughs of tomorrow.
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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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IQVIA enables genomic research via global access to a network of genomic-clinical data, proprietary technologies that enable federated analytics, and therapeutic area & bioinformatics expertise to help you answer your most pressing research questions.
LEARN MOREOur mission is to accelerate innovation for a healthier world. Together, we can solve customer challenges and improve patient lives.
LEARN MORECareers, culture and everything in between. Find out what’s going on right here, right now.
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"Improving human health requires brave thinkers who are willing to explore new ideas and build on successes. Unleash your potential with us.
SEARCH JOBSIQVIA Intelligent Document Review creates a digital twin of all your trial documents, reviews them for quality, and classifies the content so it is available in your data lake for downstream applications. The result? A seamless experience and rich insights for faster time to filing.
IQVIA Intelligent Document Review harnesses the power of AI and ML to eliminate the manual burden of populating eTMFs without sacrificing quality. With Intelligent Document Review, you can:
The traditional flow of data across the clinical trial lifecycle is a complex labyrinth of manual effort, rework, and inefficiency. IQVIA’s Intelligent Document Review brings all the content for your trial into a single, efficient stream with a clear line of sight. Rich content capture means blind spots are eliminated, and continuous quality checks ensure missing or misclassified content are spotted and corrected well in advance. Regulatory filings can even be pre-populated ahead of finalization.
The result? Earlier review and faster filing to get treatments to patients more quickly.
According to Gartner, intelligent document processing is expected to become a mainstream tool in the next two years – and those who fail to embrace it will struggle to keep pace. IQVIA’s Intelligent Document Review is on a journey to optimize data at every step of its flow, delivering faster insights, higher quality, and greater visibility across the trial lifecycle.
Learn what IQVIA Intelligent Document Review can do for your organization.
Discover intelligent insights from streamlined data and sophisticated analytics to transform trial workflows.
