
Date: Wednesday, June 17, 2026
Time: 1:00 PM – 2:30 PM EST
Registration Fee: $10
As AI-enabled systems become increasingly integrated into regulated operations, organizations must evolve governance models beyond traditional static validation approaches toward more continuous and connected assurance frameworks.
Join the ASQ Medical Device Division for a timely discussion on the practical considerations of governing AI-enabled operational environments within the medical device industry. This webinar will explore key elements of effective AI governance, including data governance, lifecycle monitoring, accountability structures, and cross-functional oversight. Attendees will also gain insight into workforce readiness, knowledge sustainability, and the importance of maintaining meaningful human judgment alongside increasing automation.
Featured speaker Filsun Moussa, Senior Regulatory Manager and Product DNA Program RA Workstream Lead at Medtronic, brings more than 15 years of experience in Regulatory Affairs and Regulatory Operations, with expertise spanning regulatory strategy, data governance, operational excellence, enterprise systems integration, and emerging technologies.
Learning Objectives
Upon completion of this webinar, participants will be able to:
- Understand how AI-enabled operational environments are expanding traditional governance and validation expectations within regulated industries.
- Identify foundational components of continuous assurance models, including data governance, monitoring, and accountability structures.
- Explore organizational considerations related to workforce readiness, knowledge sustainability, and meaningful human accountability in AI-enabled operations.
This session is ideal for professionals in Regulatory Affairs, Quality Assurance, Compliance, Digital Transformation, Product Development, and Medical Device Operations who are preparing their organizations for the future of AI-enabled environments.
Register today:
https://app.memberplanet.com/#/event/asqbiomedicaldivisioncommittee/fromreactivecompliancetocontinuousassurancegoverningaiinmedicaldeviceoperations