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Webinar on Managing Product & Process Risk through Failure Mode & Effects Analysis (FMEA)

Posted on Apr 28, 2015 1:43:00 PM

 
Seminar - Online
 
Conducted early in the process development cycle, the Failure Modes and Effects Analysis tool is used to identify risks and then adjust the manufacturing or service process to reduce the identified risks and improve quality. Attendees will learn practical application of Failure Mode and Effects Analysis (FMEA) as it is applied to product, process, or system design. The course will teach identification of potential failure modes, the risk attached and indicate their relationship to product design or manufacturing process, along with their effects, if known, on the end use of the product. Root cause analysis, risk mitigation and assessing residual risk will be addressed as part of the FMEA process. Also to be discussed are FMEA history, methods, types, responsibilities, documentation, implementation, and software. Attendees will receive an FMEA excel template that they can customize and begin immediately using.
 
Organization: Compliance Trainings (https://compliancetrainings.com)
 
Wednesday, April 29, 2015 (13:0014:00)
Mississauga, Ontario 44813, Canada
Contact: Compliance Trainings (suzzane.d@compliancetrainings.com)
Phone: 4169154458
 
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Tags: April, Webinar, Quality Control, 2015, Seminar, Biologics

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