Is your RWE ready for regulatory and payer scrutiny?
IQVIA curates and integrates fit-for-purpose real-world data with methodological rigor and therapeutic expertise. As a data-agnostic partner, we generate regulatory-grade RWE that drives submissions, market access, and adoption across lifecycles.
Access comprehensive, longitudinal health data sources
IQVIA is data agnostic—we match the right data source to your scientific and regulatory requirements. Our comprehensive longitudinal datasets cover over 318M U.S. lives, spanning claims, EMRs, patient-reported outcomes, and real-world wearables data.
Navigate regulatory complexity with seasoned experts
IQVIA's regulatory experts include former FDA reviewers and senior health economists who help navigate complex regulatory landscapes. Our team understands evolving FDA requirements and helps strengthen submissions through established regulatory precedents.
Accelerate insights with AI-powered literature analysis
AI-assisted solutions reduce manual literature review efforts by 70%. Our Healthcare-grade AI™ powers comprehensive literature analysis, evidence synthesis, and research acceleration to deliver faster, more relevant insights.
Prove economic and clinical value for payer negotiations
Generate evidence that resonates across stakeholders - from cost-effectiveness studies for payers to HCP-relevant efficacy data. We help translate RWE into targeted communications for HTAs, payers, and providers in value-based care.
Execute studies with global regulatory best practices
Operating in 100+ countries with deep regulatory filing expertise, IQVIA delivers RWE studies that meet global regulatory standards. Our best-practice approach ensures studies align with country-specific regulatory requirements and payer expectations.
Making real-world evidence regulatory-ready
At IQVIA, quality data meets expert execution. Get beyond fragmented sources. Utilize protocol-driven studies built on data spanning 1.2B+ patient lives. Let’s transform raw data into evidence that drives decisions.
IQVIA’s Real World Solutions: Accelerating Evidence, Approvals, and AI-Driven Efficiency
IQVIA’s unmatched data network, deep regulatory experience, and AI-powered tools are transforming how life sciences companies generate evidence, support approvals, and streamline research—all while maintaining scientific rigor and speed.
WHITE PAPER
Need RWE best practices for FDA filings?
Get practical guidance for your regulatory submissions that work. This white paper reveals how you can align RWE with FDA expectations using structured methodologies and fit-for-purpose data that accelerates your approvals.
Real World Evidence
From PharMetrics® Plus data to AI-powered analytics, IQVIA delivers the industry's most comprehensive RWE ecosystem.
Dig deeper into real world evidence
Find webinars, primers, and articles designed to help you grow your real world evidence knowledge base.
Discover the latest insights for Real World Evidence solutions
Real World Evidence Blog
Read our blogs for expert perspectives on the evolving role of real world data and discover our U.S. solutions.
Insights Library
Uncover expert fact sheets, briefs, and case studies on trends in Real World Evidence across the U.S.
Frequently Asked Questions
Through rigorous protocol design and fit-for-purpose data selection. We align every study with FDA and EMA guidelines, ensuring consistency from data collection through submission. Our 200+6 successful regulatory interactions prove the approach works. See our RWE best practices guide.
Deep understanding of access and reimbursement priorities. We combine health economics expertise with implementation science to create value stories that resonate. From budget impact models to outcomes analyses, we help you secure favorable coverage. Explore our implementation science approach.
By automating time-intensive processes without sacrificing quality. Our AI accelerates literature reviews by 30%, uncovers hidden insights in complex datasets, and streamlines evidence generation while maintaining full regulatory compliance. Learn about AI in evidence generation.
The industry's broadest and deepest RWD network. Access 1.2B+ patient lives through claims, EMR, hospital, lab, and specialty pharmacy data. Gain the robust data you need to support safety, outcomes, and value demonstration initiatives. Discover PharMetrics Plus.
Through our end-to-end orchestration platform. While others require you to juggle multiple vendors and systems, IQVIA provides unified project management, automated workflows, and dedicated RWE expert support. Experience seamless RWE execution.