6hr Virtual Seminar: Failure Mode and Effects Analysis for Design Improvement and Design Control
About This Event
Why Should You Attend:
Risk analysis is now required by law (GMP). Identification of device design problems prior to distribution eliminates costs associated with warranties, product recalls, and product validation.
FMEA can reveal missing requirements, missing functions, and point out component and manufacturing problems well before process validation. These in turn reduce life cycle costs and reduce the time to market. Design FMEA serves as a central document in the Design Control process Similarly the Process FMEA serves as the central document in the Process Validation qualification.
Attend this webinar to learn how you can design medical devices that enhance reliability, durability, safety, and serviceability. This seminar covers both: the Design FMEA, and the Process FMEA.
Who Will Benefit:
This webinar will provide valuable assistance to all Medical Device companies/ manufacturing sites. Those that would benefit most would be:
- R&D, Scientists
- Senior management
- Engineers
- Product Management, Product development
- Manufacturing managers and engineers
- Safety, Reliability, Quality Assurance
- Regulatory
- Purchasing & Production
- Sales and Marketing