Quality, regulatory, safety and compliance solutions across the device lifecycle.
Medical 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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