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"We strive to help improve outcomes and create a healthier, more sustainable world for people everywhere.

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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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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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"Digital Health Trends 2024 - Implications for Research and Patient Care

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"DCTs Deliver Big ROI

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"Capturing value at scale: The $4 billion RWE imperative

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Unlock your potential to drive healthcare forward

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IQVIA AI is Healthcare-grade AI

Building on a rich history of developing AI for healthcare, IQVIA AI connects the right data, technology, and expertise to address the unique needs of healthcare. It's what we call Healthcare-grade AI.

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The IQVIA Human Data Science Cloud is our unique capability designed to enable healthcare-grade analytics, tools, and data management solutions to deliver fit-for-purpose global data at scale.

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IQVIA Decentralized Trials deliver purpose-built clinical services and technologies that engage the right patients wherever they are. Our hybrid and fully virtual solutions have been used more than any others.

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Empowering patients to personalize their healthcare and connecting them to caregivers has the potential to change the care delivery paradigm.

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Webinar
Real world pharmaceutical labeling management from change trigger to implementation
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March 29, 2023

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10:00am - 11:00am

(GMT-05:00)

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  • Events and Webinars
  • Real world pharmaceutical labeling management from change trigger to implementation
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Join this webinar to gain expert advice and best practice strategies across all stages of label life cycle management - from end-to-end, label request and content management, to implementation reporting. Plus, learn about IQVIA's new management solution, which simplifies the entire labeling activity process.

You will also experience demonstrations on:

  • The use of regulatory information aggregation to assist in change impact assessment
  • The connection to and coordination of scalable content management to execute the change
  • The distribution of approved content for downstream consumption, translation, artwork creation and packaging
  • The reporting on implementation

Speakers

Cham Williams
Associate - Director, Business Systems

Julian Backhouse
Associate Director, Regulatory Technology

Hilmar Rauhe
Product Owner, Pharma Artwork

Jane Reed
Director of Life Science

Jason Berning
Associate Business Development Director (EMEA Region), Regulatory Technology Solutions

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