"Advancing obesity and obesity-related trials with patients at the center of development.
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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 ROLESIQVIA Technologies has an electronic Trial Master File that simplifies today's over-engineered products and implementations, empowering oversight without busting the budget.
The IQVIA Electronic Trial Master File (eTMF) offers precision planning and intelligent automation to create and maintain an inspection-ready eTMF that you can count on. Its simple and intuitive design minimizes manual efforts and reduces risk.
IQVIA Technologies provides an RFI/RFP template that sponsors of all sizes have used to select and evaluate the features that mean the most to them.
See your customized dashboards and metrics upon login to get immediate insights into eTMF health. Understand and correct quality, completeness, and timeliness issues proactively for nonstop audit-readiness
IQVIA eTMF streamlines day-to-day TMF document workflows, quality control (QC) checks, and finalizations for your clinical operations. Guiding team members from task to task while maintaining detailed audit trails, IQVIA eTMF keeps everyone on the same page and always prepared for health authority inspections.
This 8-minute recorded demonstration provides an overview of IQVIA eTMF Version 3. Here’s what you’ll see:
The IQVIA eTMF is part of a comprehensive suite of SaaS solutions that span the full trial continuum. We can support every aspect of trial design, start up, conduct, execution, and close out.
Reduce the high cost of administering site payments and give sites confidence.
Communication, collaboration and transparency between sites and sponsors mean trials start up and close out faster.
