Webinar Details
Title: Building Resilience in Medical Device Development: Strategies for Failure Recovery Across the Lifecycle
Description:
Unexpected technical issues are an inherent part of medical device development that can occur during any stage of the product lifecycle. While risk management aims to minimize these events, it cannot eliminate them entirely. The ability to respond effectively when issues arise is critical to maintaining project timelines, product performance, and regulatory confidence.
This webinar presents a structured, engineering-driven approach to addressing unexpected technical issues across the product lifecycle. Drawing on real-world examples, we will walk through practical strategies for overcoming technical issues and implementing effective solutions.
Key tools will be highlighted, including digital modeling, traceable requirements, and the use of development, manufacturing, and field data to accelerate root cause analysis and recovery. Attendees will gain insight into how these tools can be applied to improve decision-making, reduce iteration cycles, and increase confidence in remediation efforts.
Through case studies involving various medical devices, we will illustrate common challenges and demonstrate how a disciplined approach can turn ambiguous technical issues into actionable engineering solutions.
Speaker(s):
Catherine M. Passmore, Senior Consultant, ESi, Atlanta, GA
Nikita Pak, PhD, PE, Senior Consultant, ESi, Irvine, CA
Date: Wednesday, May 27, 2026
Time: 12:00pm-1:00pm ET
Location: Virtual
Registration: Please register using the Ticket Tailor link provided on this page.
FAQs:
Is there a cost to register for this webinar?
No, this webinar is free to attend. Registration is required, but there is no cost to participate.
Will Continuing Education (CE) be offered?
No, Continuing Education (CE) credit will not be offered for this webinar.
Will the webinar be recorded?
Yes, the webinar will be recorded. A recording will be shared with registered attendees following the session.
