Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
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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
"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 OVERVIEW
Discover new patient engagement possibilities with IQVIA insights, expertise, and technology-driven solutions.
Patient Engagement 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. IQVIA and Apple are collaborating to bring this exciting future of personalized care directly to devices patients already have and use.
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 JOBSRegulatory submissions can be a lengthy and costly process when information submitted does not meet requirements, and updates and adjustments are needed to keep drug development on track.
As experienced statisticians and programmers, we work hand-in-hand with your team with end-to-end support to help avoid late-stage delays and expedite your critical regulatory product submissions.
With stringent guidelines, it can be hard to know if your regulatory data packages are submitted with completeness and in compliance with standards.
Our highly experienced global team of programmers work across all points of data collection and analysis. From reviewing case report form design to ensuring the final define.xml packages are completed to standards with quality.
We give you confidence in your submission.
We know you need flexibility. Whether full-service or through a functional service provider (FSP) model, our team of experts can work with you every step of the way and customize efforts based on your needs. Beginning with an in-depth evaluation of current procedures and processes, we can then craft the right mix of expertise, technologies and oversight, as needed, through a flexible FSP model or full-service solution.
By heightening efficiencies in processes while also maintaining quality in what is shared with regulatory authorities, we can help ensure your innovative treatments are one step closer to reaching patients in need.
Producing Quicker and Quality Evaluations in Safety and Efficacy with Statistical Data Visualization
Manually reviewing numerous data listings line-by-line creates a time, resource and cost issue, causing your team to focus on unnecessary administrative tasks. We offer deeper visual insights into trial data and patient profiles through GRIDDS, an interactive graphical interface solution that creates a graph-based snapshot view of insights from start to database lock
Graphical displays and images are often faster and easier to relate to, facilitate pattern recognition and enable the review to rapidly identify emerging trends and outliers
High-level displays allow users to quickly grasp the big picture and follow trends, review patients disposition, demographics, monitor compliance, etc. while increasing abilities to review individual patient data
Built-in flexibility allow users to review data in a variety of formats. User-friendly reporting and collaboration capabilities further enable reviewers to track their reviews and query study data in ways that can be shared easily.
Point-and-click drill-down capabilities enable reviewers to quickly and easily home in on specific source data at the patient level, reducing the need to manually review data listings line-be-line.
Input Data Flexibility
Ability to use data from various EDC platforms, vendors data and more.
Regular Data Refreshes
Reviewers have access to patient data based on their required refresh cadence dependent on source data availability.
GRIDDS, ensures completeness, accuracy, and consistency, letting you take your time to tackle other critical issues.
Turn data into a more accurate and insightful resource with IQVIA's statistical programming team.
Advances in technology and advanced analytics have long helped other industries. Now it is happening in healthcare.
