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Smigrm 13004 Fmeawebinar

This webinar series covers the requirements for Process FMEA and Control Plans according to the AS13100 standard over three sessions. Session 1 will discuss the requirements and their link to APQP. Session 2 will explain how to properly create a Process FMEA, covering potential failures, causes, controls, and calculating RPN scores. Session 3 will introduce Reference Process FMEAs and how they can standardize PFMEAs and Control Plans to improve quality and efficiency. Each live webinar lasts two hours and allows time for Q&A.

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Mani Rathinam Rajamani
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69 views

Smigrm 13004 Fmeawebinar

This webinar series covers the requirements for Process FMEA and Control Plans according to the AS13100 standard over three sessions. Session 1 will discuss the requirements and their link to APQP. Session 2 will explain how to properly create a Process FMEA, covering potential failures, causes, controls, and calculating RPN scores. Session 3 will introduce Reference Process FMEAs and how they can standardize PFMEAs and Control Plans to improve quality and efficiency. Each live webinar lasts two hours and allows time for Q&A.

Uploaded by

Mani Rathinam Rajamani
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PPTX, PDF, TXT or read online on Scribd
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RM13004 WEBINAR SERIES

AS13100 Process FMEA & Control Plans - Meeting the Requirements while adding value to the business
Led by Dr Ian Riggs, this series of interactive webinars is designed to describe the intent of the AESQ AS13100 requirements for Process FMEA and Control Plans and how they
link to the effective deployment of Advanced Product Quality Planning (APQP) and a Zero Defect Strategy.
These webinars shall explain how AS13100 Process FMEA and Control Plans can be developed, maintained and improved using real examples of best practice from across the
industry. It shall also illustrate the unique approach to the use of Reference Process FMEAs to help standardize the organization’s PFMEAs and to reduce the length of time
taken to create them.
They will also present the opportunity to ask questions and to clarify any points around these important requirements.

SESSION 1 SESSION 2 SESSION 3


AS13100 PFMEA & Control Plan Requirements Key Elements when Creating the Process FMEA Using REFERENCE PFMEAs and Control Plans
September 14 September 15 September 16
9:00am (-5 GMT) (2 Hours) 9:00 am (-5 GMT) (2 Hours) 9:00 am (-5 GMT) (2 Hours)

Overview of the requirements for Process FMEA and Introduction to the concept of Reference Process
Control Plans in Chapter C of AS13100 and their link to A closer look at some of the key steps when creating FMEAs and how they can be used to improve the
the APQP / PPAP process Process FMEAs to illustrate the intent of the AS13100 quality and efficiency of the use of PFMEAs
requirements, including;
a) Requirements & Potential Failure Modes
Explanation of the intent of each requirement and what b) Potential Effects& Severity Rating An overview of how the Control Plan can be generated
success looks like utilizing information from the Process FMEA
c) Potential Causes
d) Prevention Controls & Occurrence Rating
Overview of the Process FMEA approach to illustrate e) Detection Controls & Detection Rating
what success looks like
f) Calculating the Risk Priority Number (RPN) Using Software to improve the use of PFMEAs and
Control Plans as part of the APQP process.
g) Prioritizing Improvements
Links to further help and guidance

Questions & Answers Questions & Answers Question and Answers

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