Thursday, Sept. 26, 2019
2 p.m. Eastern time / 11 a.m. Pacific time
Compliance issues and device recalls can cost millions of dollars, resulting in FDA warnings and irreversible damage for medical device companies. In many cases, one can trace product recalls to poor product design controls. Meeting the FDA regulations without sacrificing speed to launch products is critical. Design controls are not only a regulatory requirement — they lay the foundation for proper design and development of medical devices and provide device manufacturers with the opportunity to address issues early in the design process. Don’t miss out on this panel discussion with leading quality veterans as they share how they’ve overcome challenges meeting design controls requirements.
During this webinar, you will learn how to:
- Understand the key elements of design controls
- Determine the best approach to meet design controls requirements
- Better mitigate risk management issues
- Overcome design controls hurdles
Featured Speakers:
Ann McGuire
Manager, Product Marketing
Arena Solutions
Director of Quality Assurance
Organ Recovery Systems

Sr. Director of Quality
Nevro
Moderator
Senior Editor, Medical Design and Outsourcing