Move your business forward and take what's possible in human health further, with offerings powered by IQVIA data, analytics, technology and domain expertise
Change the model of clinical research by integrating data, expertise, analytics and technology from study design through execution to power better decisions.
Decrease clinical development costs and increase study quality using our global functional resources and flexible services, and get more value from your R&D spend.
Bring trials directly to patients to decrease costs, increase quality and improve access.
Learn more about the federated evidence networks and massive, non-identified global databases that inform our real world solutions.
Use emerging data sources and advances in evidence methods to demonstrate product value and safety.
Automate and customize data analysis and get the most out of your portfolio with scalable platforms.
Tap into evidence networks in oncology, neurology, immunology, and other therapy areas to enrich your studies.
Access clearer, more compelling support to demonstrate the value of your product.
Discover proven strategies and insights refined over more than 5,000 launches around the world.
Be proactive about growing your brand using the latest in data, analytics, and domain expertise.
Understand how payers, providers, and patients define value, and accelerate market access for new and innovative products.
Ensure your stakeholders are getting the information they need, when and where they need it, to see where your product can improve outcomes.
Effectively engage with patients to help improve adherence, drive better disease understanding, and deliver treatment value.
Harness the power of automation to execute streamlined end-to-end safety solutions while reducing costs.
Automate and standardize your regulatory management, from correspondence and commitments to registration and tracking.
From manufacturing oversight to regulatory requirements, manage quality across your organization with a single enterprise software solution.
Partner with compliance experts to create, implement and manage efficient, end-to-end processes that ensure your organization is compliant with global engagement and transparency regulations and codes.
Avoid the cost of failed sites and shorten trial timelines with evidence-based site activation and engagement technologies.
Move to streamlined, risk-based processes to manage clinical, commercial and regulatory content.
Adapt your sales strategies and field force to meet the demands precision medicine creates for more precision and deeper information.
Get an overview of IQVIA's full range of solutions to help you work more efficiently, standardize and improve controls across development stages and geographies.
Get alignment on what to measure, eliminate duplicative reporting and make complex data easier to manage with our easy-to-deploy analytics suite.
Partnering with pharmacy and wholesalers to support their business needs.
Learn how unparalleled data, domain expertise, and technologies enable AI-powered solutions that are purpose-built for healthcare.
Boost recruitment and retention, speed timelines, improve data quality. Bring trials and real world studies to patients at home with IQVIA Virtual Research.
Learn how IQVIA is unlocking genomic data, at scale, while preserving privacy. Enabling a faster, more flexible, and less expensive approach for scientific enquiry into human biology, drug discovery and drug development.
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.
Access broad and deep neurology expertise to reduce costs, accelerate timelines and manage risk, from clinical trials to evidence generation and beyond.
Leverage numerous infectious disease and vaccine experts using best-in-class data sources and the right sites.