Regulatory & Standards Landscape for AI in Healthcare

When:  Feb 10, 2026 from 05:30 PM to 06:30 PM (CT)
Associated with  Medical Device Division

Artificial Intelligence is an impressively fast-moving technology in all fields, especially for medical devices. It is already improving patient lives with innovative healthcare, lower healthcare costs, and better patient outcomes, but as with all advances, if not properly regulated, these benefits could possibly open risks to safety and security.

Please join Pat Baird, Senior Regulatory Specialist at Philips, as he addresses new and emerging regulations and standards (both national and international), and where this technology will take us in the next few years.

REGISTRATION REQUIRED:  

Venue:  Zoom/Online Event. Zoom Link will be provided closer to the event date.

Date: Tuesday, February 10, 2026

Time:  5:30 pm – 6:30 pm CST

Cost:  $15        

THE EMAIL USED DURING REGISTRATION IS THE EMAIL USED FOR ALL EVENT COMMUNICATION INCLUDING THE ZOOM LINK.

Certificates of Completion: Issued via email, after event completion, for .1 ASQ RUs or .1 CEUs

QuestionsPlease contact Karen Peifer, Committee Chair, at asqmnbmc@gmail.com

Your Speaker

Pat Baird, Senior Regulatory Specialist at Philips

Pat Baird works at Philips as a Software Standards Specialist, with a focus on the use of AI in healthcare. Pat likes to think of his job as “Policy Engineering” – understanding the unmet needs (and frustrations) of regulators and developers, and developing standards, whitepapers, and training to meet those needs. Past roles have included software developer, engineering manager, project manager, lead engineer, and Director of Risk Management before getting involved in regulatory & standards. He co-chairs multiple committees related to artificial intelligence at AAMI, ISO, CTA, AdvaMed, and AFDO/RAPS, and is involved with other software committees regarding topics such as cloud services for a regulated environment, risk management, cybersecurity, and is a sub-team lead for the IMDRF AI for Medical Devices committee; Pat also was one of the authors of the RAPS Software as a Medical Device book.

Sponsor Information

The MN ASQ Biomedical Consortium (BMC) is a group of quality professionals promoting and advancing quality tools, principles, and practices through educational events.  We focus on the medical device industry but promote events for other regulated environments. 

·      Follow us on LinkedIn to stay informed of upcoming events:  https://www.linkedin.com/showcase/90642322/

To become a member of the MN ASQ Biomedical Consortium, please contact Karen Peifer, Committee Chair or Sahi Datla, Committee Co-Chair, at asqmnbmc@gmail.com.

The American Society for Quality (ASQ), is a knowledge-based global community of quality professionals, with nearly 80,000 members dedicated to promoting and advancing quality tools, principles, and practices in their workplaces and communities.  As your career partner, ASQ membership benefits are designed to help meet your growing needs as a quality professional.  Membership provides exclusive access to quality knowledge, solutions, and resources to solve challenges, and skill development to advance your career. ASQ is committed to providing enhanced expertise, professional networks, tools, and solutions to help our members advance their products, services, and industries.

ASQ:  https://www.asq.org/ 

Location

Online Instructions:
Url: https://mp.gg/mtj9hho7
Login: Registrants will receive the Zoom link closer to the event date.
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Contact

Karen Peifer

asqmnbmc@gmail.com