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EMEA Thought Leadership
Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
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Americas
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Asia & Oceania
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Europe
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Americas
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Asia & Oceania
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EMEA Thought Leadership
Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
Learn more -
Middle East & Africa
EMEA Thought Leadership
Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
Learn more
WHO WE HELP
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Pharmaceutical Manufacturers
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Pharmaceutical Manufacturers
Harness unparalleled healthcare data, advanced analytics, and cutting-edge technologies with our expertise to accelerate the development and commercialization of innovative medicines, enhancing patient lives.
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Emerging Biopharma (Global page)
Boost your innovation with IQVIA's expert team. Our comprehensive solutions integrate top-tier insights, technology, and expertise to maximize your asset's success in a competitive landscape.
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Leverage digital innovation to cut costs, boost efficiency, and elevate patient engagement, all while enhancing quality and health outcomes.
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Insurers and Risk
Enhance your ability to evaluate and forecast population risk swiftly and accurately by integrating unmatched data, expertise, and technology.
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Medical Specialty and Patient Advocacy
Transform into a data-driven organization that enhances your specialty and showcases value to your members through digital transformation.
Explore NowU.S. PROGRESS POINT
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EXPLORE PODCASTSFact Sheet
Unlocking Success in Drug Development with External Comparators
IQVIA’s expert guidance and advanced methodologies can enhance the design of external comparators for regulatory decisions
May 27, 2024
The use of external comparators (ECs) in drug development is on the rise, fueled by real-world data (RWD) and advancements in personalized medicine. Notably, the period from 2015 to 2019 saw a 22% increase in RWD-based EC usage. This upward trend is expected to continue, especially following the FDA’s February 2023 draft guidance, which advocates for a nuanced, case-by-case assessment of EC cohort designs.
While EC studies can significantly augment product lifecycles, from streamlining clinical trial design to strengthening real-world evidence (RWE) for payor negotiations and market positioning, the question arises: How can sponsors effectively advocate for their utilization to address the needs of a drug development program?