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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.
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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.
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Elevate commercial models with precision and speed using AI-driven analytics and technology that illuminate hidden insights in data.
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Orchestrate your success across the complete compliance lifecycle with best-in-class services and solutions for safety, regulatory, quality and medical information.
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When your destination is a healthier world, making intelligent connections between data, technology, and services is your roadmap.
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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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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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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.
VIEW ROLESEvaluate how trials can be run quicker using new biostatistical methods
Applied case study example of study design using the latest tools and methodologies
- Phase-3 oncology design as a case study
- Latest AI/ML tools to leverage Phase-2 study data to set patient inclusion/exclusion criterion for broadest possible label as well as increase probability of study success. This also potentially reduces cost and time to run trial
- Use of latest adaptive trial design innovations to reduce trial cost, risk, and time
- Adaptive accrual to incorporate actual response and hazard rates for efficient trial execution without sacrificing power
- Case study wrap-up from clinician's perspective with all these efficiencies and optimizations
Join our upcoming webinar on October 25, and hear IQVIA’s VP Biostatistics Russ Reeve and AI/ML expert Kal Chaudhuri as they sets out to highlight how applied adaptive design using subgroup identification & machine learning can reduce trial risk, cost and runtime. Sign up now, and learn how to optimize your workflow using biostatistics and ML.
Register here https://globalmeet.webcasts.com/starthere.jsp?ei=1568893&tp_key=ed851ed0c6&sti=iqvia