Benefits of AI in Medical Device Manufacturing and Considerations for Responsible, Compliant Deployment

Available On-Demand

AI is moving quickly, but in medical device manufacturing, deployment success can involve validation, compliance, and control.

In this On-Demand webinar, you’ll learn how to shift from a System of Record to a System of Action, where AI supports real-time decisions across quality, production, and supply chain—without compromising GMP requirements.

Built on the #1 platform for manufacturers, and powered by ChampionAI, this session focuses on practical frameworks you can apply immediately in regulated environments.


View this On-Demand webinar to learn:
  • What FDA and EU regulators expect for AI-enabled systems
  • How to approach validation, risk management, and ongoing performance monitoring
  • Where AI is being applied first (quality, supply chain, production)
  • How manufacturers are moving from pilot to compliant, production-ready deployment
  • A real-world example and how ChampionAI support execution

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Speakers

Robyn CowardHeadshot-Robyn-Coward.png
Life Sciences Director, QAD
Robyn is the Life Sciences Director at QAD. With 21 years of experience in product commercialization, Robyn has spent the last 11 years focused on the global life sciences markets, particularly in the imaging, laboratory diagnostics, and healthcare IT segments.

 
 
Daljit Chaggar
Regional VP Compliance, NNIT
Daljit brings over two decades of experience in Quality, Compliance, and Validation, supporting global life sciences organizations. Known for a pragmatic yet strategic approach, she combines strong analytical and risk mitigation skills with hands-on validation execution and deep regulatory insight aligned with FDA and EU standards.