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 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 Activity Schedule Designer helps customers create an optimal schedule of activities, reducing study costs and timelines, eliminating unnecessary patient burden and preventing avoidable protocol amendments.
A cloud-based, data-driven solution, IQVIA Activity Schedule Designer (ASD) helps life sciences companies and CROs create an optimal schedule of trial activities to accurately predict and heighten study performance. Driven by IQVIA Connected Intelligence™, ASD enables improved study design and drives trial efficiencies, reducing protocol amendments and improving the patient experience, thus minimizing unplanned costs and time delays.
ASD helps us assess our protocols in a unique manner by allowing us to quantify patient/site burden and identify non-essential procedures to improve study cost management & operational feasibility.
Using Activity Schedule Designer, the schedule of activities is mapped to study endpoints and objectives. Study teams create documented, reusable scenarios for visits and activities which are iterated by cross-functional teams in design sessions. They weigh country options and enrollment benchmarks against study criteria.
ASD helps users identify and eliminate non-core procedures and non-essential patient visits to save money and time.
Users create and iterate on an ideal visit structure, applying proprietary scoring methodology to identify patient burden at the visit, procedure and study level and highlighting barriers to patient recruitment and retention.
ASD applies GrantPlan, the industry’s largest benchmark dataset of procedure and activity cost data, to the schedule of activities to further enable cost transparency.
Flexible cost configuration allows views and analysis in multiple ways – by country, patient endpoint, cross-countries, and more.
Better match investigators and sites to trial objectives
Improve and accelerate site vetting and selection processes.
Build better study budgets while reducing costs and improving start-up times – accurately and compliantly
Accurately predict study timeline, budget, and performance.
