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Failure Mode and Effects Analysis for Design Improvement and Design Control

Failure Mode and Effects Analysis for Design Improvement and Design Control

Venue Name: Online Event
Country: United States of America
City: Palo Alto
State: california
Number of Attendees: Unknown
Webinar or Virtual Event: Yes
Keywords: R&D, Scientists, Senior management, Engineers, Failure Mode and Effects Analysis, FMEA for Medical Devices, FMEA for Design Improvement, FMEA for Design Control
Start Date of Conference:: 11-07-2011
End Date of Conference: 11-07-2011
Description of Conference: In this Failure Mode and Effects Analysis training, learn how you can design medical devices that enhance reliability, durability, safety, and serviceability. Get a solid understanding of both the Design FMEA, and the Process FMEA.

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.

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
- Suppliers


NOTE : Use this Promocode (128600)to avail 10% discount,Valid till December 30 & add another webinar to your shopping cart and get 20% off on its price

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