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Wed November 4, 2015

Failure Mode and Effects Analysis for Design Improvement and Design Control

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at Online - Webinar (see times)
Topic ID: 000000200-web

Start Date: Nov 4, 2015

Start Time: 10 AM PST | 1 PM EST

Name of Event: Failure Mode and Effects Analysis for Design Improvement and Design Control

Details: 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.

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.

Areas Covered In The Session:
FMEA methodology-the right way
Design FMEA Procedure
Developing Elegant Design Solutions
Process FMECA Procedure
FMEA for Planning Design Validation
FMEA for Planning Process Validation

Speaker: Dev Raheja, MS,CSP, is an international Risk Management and Quality Assurance consultant for Healthcare,medical device, and aerospace industry for over 25 years. He applies evidence base safety techniques from a variety of industries to healthcare. He is a trainer, author of the books Safer Hospital Care, Assurance Technologies Principles and Practices, and Design for Reliability. He shows clients how to come up with elegant solutions using creativity and innovation. Being a true international consultant, he has conducted training in several countries including Sweden, Australia, Japan, Germany, UK, Singapore, Taiwan, South Africa, Finland, and Brazil. He helped a major Midwest company from going out of business to becoming a world leader by eliminating safety mishaps. Prior to be coming a consultant in 1982 he worked at GE healthcare as Supervisor of Quality Assurance and Manager of Manufacturing, and at Booz-Allen &Hamilton as Risk Management consultant for nuclear and mass transportation industry.

For more details call Complystream at: (+1) 844 498 6361
Topic ID: 000000200-web

Start Date: Nov 4, 2015

Start Time: 10 AM PST | 1 PM EST

Name of Event: Failure Mode and Effects Analysis for Design Improvement and Design Control

Details: 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.

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.

Areas Covered In The Session:
FMEA methodology-the right way
Design FMEA Procedure
Developing Elegant Design Solutions
Process FMECA Procedure
FMEA for Planning Design Validation
FMEA for Planning Process Validation

Speaker: Dev Raheja, MS,CSP, is an international Risk Management and Quality Assurance consultant for Healthcare,medical device, and aerospace industry for over 25 years. He applies evidence base safety techniques from a variety of industries to healthcare. He is a trainer, author of the books Safer Hospital Care, Assurance Technologies Principles and Practices, and Design for Reliability. He shows clients how to come up with elegant solutions using creativity and innovation. Being a true international consultant, he has conducted training in several countries including Sweden, Australia, Japan, Germany, UK, Singapore, Taiwan, South Africa, Finland, and Brazil. He helped a major Midwest company from going out of business to becoming a world leader by eliminating safety mishaps. Prior to be coming a consultant in 1982 he worked at GE healthcare as Supervisor of Quality Assurance and Manager of Manufacturing, and at Booz-Allen &Hamilton as Risk Management consultant for nuclear and mass transportation industry.

For more details call Complystream at: (+1) 844 498 6361
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Online - Webinar
420 Lexington Avenue Suite 300, New York City, NY 10170

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