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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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Elevate commercial models with precision and speed using AI-driven analytics and technology that illuminate hidden insights in data.
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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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When your destination is a healthier world, making intelligent connections between data, technology, and services is your roadmap.
TECHNOLOGIES OVERVIEWExplore our library of insights, thought leadership, and the latest topics & trends in healthcare.
DISCOVER INSIGHTSAn in-depth exploration of the global healthcare ecosystem with timely research, insightful analysis, and scientific expertise.
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By making intelligent connections between your needs, our capabilities, and the healthcare ecosystem, we can help you be more agile, accelerate results, and improve patient outcomes.
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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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Your new expert analyst is here. Be at the forefront of data-driven decision-making with a new generative AI tool that enables you to interact with our products and solutions like never before. Get results you can trust, faster.
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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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The IQVIA Innovation Hub connects start-ups with the extensive IQVIA network of assets, resources, clients, and partners. Together, we can help lead the future of healthcare with the extensive IQVIA network of assets, resources, clients, and partners.
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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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"At IQVIA your potential has no limits. We thrive on bold ideas and fearless innovation. Join us in reimagining what’s possible.
VIEW ROLESMedical Device and In-Vitro Diagnostic (IVD) organizations continue to face many challenges, including the increasingly rapid pace of innovation and a constantly evolving regulatory environment. These are further complicated by the need for robust post-market surveillance, which has seen increased scrutiny under the European Medical Device and IVD Regulations (EU MDR and EU IVDR).
At the same time, AI innovations—including Machine Learning (ML), Generative AI (GenAI), and Agentic AI—can enhance efficiency and effectiveness across Medical Devices and IVD functions, such as quality, regulatory, safety, and medical affairs. This enables accelerated innovation, an enhanced focus on patient safety and product quality, and improved decision-making.
Join IQVIA’s Jane Reed, PhD., Director, Applied AI Science, and Mike King, Senior Director, Product & Strategy, MedTech, for a live presentation and Q&A that will explore the transformative potential of AI for Medical Device and IVD organizations.
You’ll see several real-world examples from IQVIA that showcase the application of AI in Medical Devices and IVDs, such as improving medical device safety, evaluating post-market device performance, and enhancing competitive intelligence.
Key learnings:
Jane Reed leads sales enablement and strategy for IQVIA’s Applied AI Science (AAIS) offerings in pharma, healthcare, and MedTech, focusing on safety and regulatory affairs. With 20+ years’ experience supplying data, technology, and analytics to pharma and biotech via roles at Instem, BioWisdom, and Incyte, Jane holds a PhD. from Birmingham University with post-docs in genetics and genomics.
Mike King has spent ~ 20 years leading localized and global teams in regulatory affairs and quality assurance, working within the medical and surgical, orthopedic, in-vitro diagnostic, diagnostic imaging, dental, and urology sectors. His focus is optimizing business workflows through intelligence-driven simplification and automation within and across the quality, regulatory, and safety functions.
Quality, regulatory, safety and compliance solutions across the device lifecycle.
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