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"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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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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Your new expert analyst is here. Be at the forefront of data-driven decision-making with a new generative AI tool that enables you to interact with our products and solutions like never before. Get results you can trust, faster.
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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 ROLESImprove study outcomes for pediatric therapies by addressing the needs of children and their families –
from formulations to biospecimen requirements.
Pediatric expertise is essential to developing and commercializing pediatric therapies, from the earliest planning stages through launch and real-world assessment. With our Pediatric Center of Excellence, we provide a range of scientific, therapeutic, regulatory, and operational expertise to ensure study success.
These resources extend beyond IQVIA to encompass a global network of top performing sites, ensuring there are sites around the world with the proven ability to conduct every pediatric clinical trial.
Conduct thorough independent audits of study documents and processes to identify specific pediatric considerations and safeguard the well-being of children in research.
Utilize pharmacokinetic modeling and simulations to minimize lab procedures for children, which reduces anxiety and increases retention.
Drug formulations that are palatable to young children, such as dispersible and mini tablets, improve adherence and safety among patients.
IQVIA CTEs help onboard patients into studies, share expertise, and advocate for them and their families, which improve outcomes.
Offer the flexibility and convenience of hybrid and decentralized clinical trial modalities to reduce burden for pediatric patients and their families.
Navigate the landscape of consent regulations that vary by age and country, and demonstrate concern for patient rights, privacy and custody issues.
Collaborate with PAGs to raise study awareness and facilitate patient and family participation in aspects of studies including protocol design and relevant endpoints.
Successful pediatric trial designs are attentive to the needs of infant, child, or adolescent patients. And decision making about study participation typically involves multiple family members.
IQVIA considers the differences within pediatric sub-populations and takes a sensitive approach to these patients and their caregivers.
activated for various pediatric trials
implemented in 101 countries since 2018
in studies, including pediatric patients
published by IQVIA, including six in oncology and seven in immunology
Build on our experience of more than 245 rare disease studies in 96 countries to fulfill your promise of hope to millions around the world.
Identify the best performing sites for your trial in less time with new machine learning and predictive modeling methods.
Bring trials directly to patients to improve access and engagement, increase quality and shorten timelines.
