"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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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 ROLESStreamline your drug development process and reduce time-to-market with an integrated asset development framework. From early-stage research to late-stage commercialization, we leverage AI technologies to enhance the strategic guidance and support needed to clear regulatory hurdles, design robust clinical trials and develop effective market entry strategies.
By combining regulatory, clinical, and commercial strategies with advanced AI/ML analytics and methodologies, we improve the efficiency and effectiveness of your drug development. Leverage Healthcare Grade AI® throughout your strategic planning — from prioritizing the best indications for your asset through operational feasibility assessments. Manage changing market conditions and stakeholder needs effectively with Integrated Asset Development solutions.
Choosing the right indication for a new therapeutic is a crucial decision that can involve numerous possibilities. Our experts help you prioritize indications not just based on scientific rationale, but also by considering the complexities of clinical development, regulatory strategy and commercial potential. Guide your drug development journey with a comprehensive view of disease landscapes, competitive environments and market opportunities.
Your Target Product Profile is a strategic planning tool that outlines your product’s critical attributes, from efficacy and safety to manufacturing and pricing. Defining these attributes early on fosters stakeholder alignment, facilitates efficient resource allocation, and increases the likelihood of developing a successful product. Our experts will delve into the intricacies of your product — understanding its unique strengths and potential applications — and align these insights with market needs, regulatory requirements and competitive landscapes, resulting in a clear, compelling profile.
Assure your product safety and effectiveness before it enters clinical trials. Work with a dedicated team who understands the complexities of non-clinical development activities, including safety assessments, toxicology and pharmacokinetics / pharmacodynamics (PK/PD) aspects. Get the critical insights you need to inform the design and execution of your clinical development program.
Ensure your product's unique attributes and market objectives are met with a tailored clinical development plan. Strategic guidance on study design, patient population selection, endpoints determination and regulatory strategy allow you to make evidence-based decisions for your clinical development program. By outlining a clear strategy, setting realistic goals and preparing for potential risks, you can increase the likelihood of your product’s success.
Representative practices in clinical trials is essential for ensuring products are safe and effective for all populations. Address gaps in care by reaching the minority subgroups most impacted by the disease state within your clinical trial. Targeted recruitment and retention strategies that extend from action plans through study design and site selection ensure your therapy meets the needs of the patients who need it most.
