Usability Principles for Medical Devices: Interpreting and Implementing IEC 62366 Webinar
DUBLIN, Nov. 16, 2023 /PRNewswire/ -- The "4-Hour Virtual Seminar on Usability Principles for Medical Devices: Interpreting and Implementing IEC 62366" webinar has been added to ResearchAndMarkets.com's offering.
Discover the Power of IEC 62366-1's 9-Stage Model for Regulated Companies. Are you ready to take your product development and implementation to the next level? Join our high-impact seminar, designed to equip your company with valuable guidance on incorporating Use Engineering / Human Factors Engineering using the acclaimed IEC 62366-1 framework.
Why Should You Attend:
Both the U.S. FDA and the EU's MDR mandate the consideration of Use Engineering / Human Factors Engineering for new or updated products. Don't let compliance become a stumbling block; instead, be proactive in evaluating your device's interface and empower your team to design products that users will love.
Harness the Full Potential of Use Engineering! Unravel the mystery behind the nine stages of Use Engineering, and learn how to provide foolproof documentation to demonstrate compliance. Equip your product engineers with the knowledge to refine designs for optimal usability, risk reduction, and customer satisfaction.
Key Topics Covered:
He specializes in quality assurance, regulatory affairs, QMS problem remediation and FDA responses, new/changed product 510(k)s, process/product/equipment QMS and software validations, ISO 14971 product risk management files/reports, Design Control/Design History Files, Technical Files, CAPA systems and analysis.
He has published numerous articles in peer reviewed journals, conducted workshops and webinars worldwide on CAPA, 510(k)s, risk analysis/management, FDA/GMP audits, validation, root cause analysis, and others. He writes a recurring column for the Journal of Validation Technology. John is a graduate of UCLA.
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