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Impacting People's Lives
Harness the power to transform clinical development
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.
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Real World Evidence. Real Confidence. Real Results.
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.
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Elevate commercial models with precision and speed using AI-driven analytics and technology that illuminate hidden insights in data.
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Service driven. Tech-enabled. Integrated compliance.
Orchestrate your success across the complete compliance lifecycle with best-in-class services and solutions for safety, regulatory, quality and medical information.
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Intelligence that transforms life sciences end-to-end.
When your destination is a healthier world, making intelligent connections between data, technology, and services is your roadmap.
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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.
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Explore IQVIA by region
As a global community, IQVIA continuously invests and commits to advancing human health.
Americas
Europe
Asia & Oceania
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EMEA Thought Leadership
White Paper
Efficient Real World Evidence Generation with Enriched Methods
Bringing primary and secondary data together for real world studies and trials
Dec 14, 2021
- Library
- Efficient Real World Evidence Generation with Enriched Methods
By combining primary data collected directly from study sites, patients, or health care providers with secondary data such as electronic medical records (EMRs) or administrative claims data, enriched studies can increase the amount of researchable data and may allow more scientific questions to be addressed in a single study.
Enriched data collection methods may be applied to a range of study designs and research objectives, including Virtual Trials, Disease and Product Registries, Extension Studies, Post Authorization Safety Studies (PASS), Post Authorization Efficacy Studies (PAES), Randomized Pragmatic Studies, and Drug Utilization Studies (DUS).
Related solutions
Study Design
Use emerging data sources and advances in evidence methods to demonstrate product value and safety.
Real World Evidence
IQVIA is using vast quantities of data in powerful new ways. See how we can help you tap into information from past trials, patient reported outcomes and other sources to accelerate your research.