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 JOBSCell and gene therapies offer tremendous promise where traditional treatments fall short. These innovative therapies require charting new, riskier territory. Our multi-disciplinary cell and gene therapy teams are poised to help you bring life changing treatments to patients earlier.
We have a unique perspective across the landscape of Cell and Gene Therapy (CAGT). We work extensively with both biotech and large pharma customer and draw upon our broad experiences to craft tailored solutions to help sponsors optimize and accelerate their clinical development.
This is who we are, what we do, and how we're different.
Our expert CAGT Medical and Scientific Team advise sponsors on all aspects of CAGT clinical development
Our CAGT Center of Excellence includes highly experienced physicians and clinical operational experts with direct medical, scientific and clinical development experience in CAGT. We harness IQVIA data and innovations and advise on protocol design, regulatory, clinical operations, real-world evidence needs, specialized lab requirements, and commercialization strategies.
We craft tailored strategies for all aspects of CAGT clinical development, especially clinical trials. We work in partnership with our CAGT clinical operations teams and other IQVIA indication-specific Centers of Excellence.
Our specialized CAGT Clinical Operations and Logistics Management teams expertly deliver CAGT trials.
CAGT trials demand meticulous delivery and management of logistics. We have first in class solutions to optimize CAGT study execution.
For our biotech customers, we have developed an innovative, multi-disciplinary CAGT unit, in which the CAGT Center of Excellence partners with an experienced CAGT clinical operations team to ensure seamless clinical program strategy and delivery.
Our Logistics Management Program features experienced logistics managers, supply chain teams, and partnerships with shipping vendors. We are also experienced in the latest tracking tools and innovations in Chain of Custody/Identity verification.
We leverage data-driven insights and established relationships to identify the best sites.
Our global CAGT site network includes more than 160 sites around the globe, including experienced sites in Asia-Pacific and Latin America. Our CAGT sites have expert research teams, infrastructure for cell and gene therapies, and the necessary CAGT certifications.
We use patient-centered and data-driven approaches to identify and recruit patients
CAGT trials often involve rare, pediatric, and patients with advanced disease. We use patient-centered strategies to ensure patient burden is minimized and proprietary IQVIA data to optimize and accelerate recruitment of these challenging populations.
Our patient engagement toolbox includes tailored CAGT recruitment materials, concierge services, and electronic consent. We also leverage our extensive data and biomarker networks to find and identify eligible patients. Finally, we use innovative approaches to minimize patient burden including decentralized trials and remote data collection.
We use innovative study designs and leverage real world data to streamline CAGT long term follow up
Real world evidence is critical to many aspects of CAGT clinical development. We work in partnership with our Real-World Solutions teams to craft innovative study designs and strategies for long term follow up, natural history studies, and external comparator studies. We also leverage our real-world solutions to inform payor and commercialization strategies.
We provide regulatory strategy, advice, and consulting from pre-registration to post-registration. Our program includes a wide range of services including regulatory intelligence, regulatory maintenance and lifecycle support, marketing applications, accelerated approval designations, INTERACT/Pre-IND/IND consultation, prioritization and target product profiles.
We provide CMC strategy, labeling, and GMP compliance audit support. We also provide Pre-IND and scientific advice meeting consultation. Through an award from the California Institute for Regenerative Medicine (CIRM), we provide pre-clinical services to CIRM grantees.
IQVIA’s Q2 Lab Solutions offers an extensive array of CAGT lab solutions to meet the unique demands of CAGT clinical development.
Our CAGT Center of Excellence works in collaboration with Q2 solutions scientists and operational teams develop bespoke lab strategies informed by specific clinical needs.
Our powerful approach brings together CAGT experts, data-driven insights, global site networks, and innovative technologies to help you drive smarter decisions to accelerate CAGT clinical development.
Discover how IQVIA Biotech can build tailored solutions for biotech companies throughout the drug development journey.
Generate and disseminate the right real world evidence (RWE) to meet stakeholder needs with confidence.
IQVIA Decentralized Trials deliver purpose-built clinical services and technologies that engage the right patients wherever they are.
Predict enrollment more accurately and increase the number of patients per site using data-driven patient recruitment solutions.
