IQVIA’s cover photo
IQVIA

IQVIA

Hospitals and Health Care

Durham, North Carolina 2,262,220 followers

Accelerate innovation for a healthier world.

About us

IQVIA (NYSE:IQV) is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. IQVIA’s portfolio of solutions are powered by IQVIA Connected Intelligence™ to deliver actionable insights and services built on high-quality health data, Healthcare-grade AI™, advanced analytics, the latest technologies and extensive domain expertise. With approximately 88,000 employees in over 100 countries, including experts in healthcare, life sciences, data science, technology and operational excellence, IQVIA is dedicated to accelerating the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. IQVIA is a global leader in protecting individual patient privacy. The company uses a wide variety of privacy-enhancing technologies and safeguards to protect individual privacy while generating and analyzing information on a scale that helps healthcare stakeholders identify disease patterns and correlate with the precise treatment path and therapy needed for better outcomes. IQVIA’s insights and execution capabilities help biotech, medical device and pharmaceutical companies, medical researchers, government agencies, payers and other healthcare stakeholders tap into a deeper understanding of diseases, human behaviors and scientific progress, in an effort to advance healthcare. To learn more, visit www.iqvia.com.

Industry
Hospitals and Health Care
Company size
10,001+ employees
Headquarters
Durham, North Carolina
Type
Public Company
Specialties
Technology, Consulting, and Clinical Development

Locations

Employees at IQVIA

Updates

  • View organization page for IQVIA

    2,262,220 followers

    We are proud to share that IQVIA’s Dr Joanne M. Hackett and Marie E Lamont have been respectively named Healthcare Businesswomen’s Association (HBA) 2025 award winners! The HBA awards honor women in healthcare for their significant contributions, leadership, mentorship, and innovative impact: congratulations to Joanne and Marie for your achievement and for the inspiring example you set. Learn more: https://bit.ly/4jrKnOj

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  • View organization page for IQVIA

    2,262,220 followers

    The use of Real World Evidence (RWE) and externally controlled trials (ECTs) are increasingly relevant for obtaining marketing authorizations for drugs in research and development. In this article in Clinical Researcher, IQVIA’s Reid D'Amico, Ph.D. D’Amico discusses best practices to help sponsors effectively navigate the regulatory landscape and leverage RWE to support their submissions. https://bit.ly/4jVvxzC

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  • View organization page for IQVIA

    2,262,220 followers

    Last chance to register!

    View organization page for IQVIA United States

    22,497 followers

    Don't miss our upcoming webinar on May 1 at 12pm ET titled "A SMART Approach to Healthcare Innovation Using Fast Healthcare Interoperability Resources." Learn how to solve interoperability challenges and transform healthcare data exchange: https://bit.ly/3ErAuRu Discussion Highlights: • Key challenges in healthcare interoperability • Robust data privacy and security measures • Implementation strategies and success stories

  • View organization page for IQVIA

    2,262,220 followers

    Connect with us at ISPOR Montreal! We’re looking forward to talking with you. Meet our team and learn more about our latest RWE, Market Access and HEOR insights. We’ll feature live demos of IQVIA’s best-in-class technologies, including AI-Assisted Scientific Literature Review, Market Access Insights and OMOP Analytics, as well as 46 posters featuring our research. Learn more: https://bit.ly/431mjvY

  • View organization page for IQVIA

    2,262,220 followers

    Discover the future of pharmacovigilance and regulatory compliance with IQVIA's "The Future of Pharmacovigilance: Integrating AI with Drug Safety Systems" white paper. This comprehensive guide offers insights into the future of PV, including understanding the FDA's Emerging Drug Safety Technology Program (EDSTP), discovering how AI can enhance PV processes by improving efficiency, accuracy, and compliance, and learning from real-world examples of successful AI integration into PV systems to position your organization as a leader in PV innovation.

    View organization page for IQVIA Safety & Regulatory Compliance

    21,117 followers

    At IQVIA, we are at the forefront of integrating artificial intelligence (AI) into pharmacovigilance (PV) processes to enhance efficiency, accuracy, and patient outcomes. Our latest white paper, "The Future of Pharmacovigilance: Integrating AI with Drug Safety Systems," explores the ground-breaking potential of AI in PV, guided by the FDA's Emerging Drug Safety Technology Program (EDSTP). Discover how AI can streamline case processing, improve adverse event intake, and navigate the evolving regulatory landscape. Learn from our experts, Archana Hegde and Updesh Dosanjh, about strategic implementation and the latest regulatory guidance to ensure compliance and maximize the benefits of AI in drug safety. Read the full white paper here: https://bit.ly/3Rjqf4K #Pharmacovigilance #AI #DrugSafety #FDA #EDSTP

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  • View organization page for IQVIA

    2,262,220 followers

    Dive into the future with IQVIA Laboratories Genomics, a leader in comprehensive lab and bioinformatics services for drug discovery, clinical development, and precision medicine. With state-of-the-art facilities in the U.S., U.K., China, and Singapore, they offer custom assay design, validation, clinical sample analysis, and bioinformatics data analysis. Learn more below!

    View organization page for IQVIA Laboratories

    52,240 followers

    Our expert team at IQVIA Laboratories Genomics offers comprehensive lab and bioinformatics services for drug discovery, clinical development, and precision medicine. With facilities in the U.S., U.K., China, and Singapore, we provide custom assay design, validation, clinical sample analysis, and bioinformatics data analysis. Visit our website to learn more! https://bit.ly/3RtnrBZ

  • View organization page for IQVIA

    2,262,220 followers

    For researchers and data providers, documentation needs for real world evidence submissions to regulators can be ambiguous. A dynamic framework recently developed by leaders from the International Society for Pharmacoepidemiology, the Professional Society for Health Economics and Outcomes Research, and TransCelerate, including Christina Mack, Cynthia Girman, Rachel Leahy, PhD, RAC, Dana Teltsch, Morgan Marks, Grazyna Lieberman, Molly (Lorton) Aldridge, and Chris Atzinger, can help by highlighting clarifying important details needed for FDA submissions. Read the article: https://bit.ly/4cOyIXB

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Funding

IQVIA 3 total rounds

Last Round

Post IPO debt

US$ 500.0M

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