Is the 8D process a part of QS-9000? SEC:U 8D

D

David Mullins

#1
SEC:U 8D

I received the following questions from a student doing a project on FORD 8D. If you could share your answers on these I'm sure he would appreciate it. (I thought a broader perspective might help)

Is the 8D process a part of QS9000 or is it a tool to help companies abide by the standard?

It isn't only used by Auto companies though is it? It can be applied in other types of
industries eg computers can it?

I've heard of the Seven Step problem solving method which is similar to the 8D problem solving model. Do you know of any others?



------------------
 
Elsmar Forum Sponsor
B

Bill M

#2
The 8 Discipline or 8D is a formal problem solving methodology that Ford uses as a part of their Team Oriented Problem Solving (TOPS). It is widely adopted and many companies within and outside the automotive industry have similar formats with some variations. The Chrysler 7 Step is basically the 8D without the last step; "congratulate the team". Another system is the 5 Phase or 5P. The 8D is part of QS-9000 by way of the requirement that a supplier must respond to a customer concern in the format the customer has designated. Therefore all Ford suppliers would use the 8D to address Ford concerns. Similar formats are in use in a form most companies know as a Corrective Action Report...simply put it would be a form with the basic steps: 1. What is the concern? 2. Who's assigned to deal with the concern? 3. What steps (immediate and long term) are to be taken to address the root cause of the concern and will prevent it from recurring? 4. Afterwards, what was done to verify that it is not still a concern? 5. Closure or Sign-offs
 
D

dewie

#4
To do effective corrective & preventive action, I used to suggest the 8D concept to many industries include servicing business. My friend who is an instructor in university said this is a good concept of step by step problem solving.
 
Thread starter Similar threads Forum Replies Date
T GRR based on part tolerance or process variation. Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 7
M Are Risks and Opportunities Required as Part of the Process Definition ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 3
D Has anyone undergone a BARDA (HHS) audit as part of their grant process? Other Medical Device Regulations World-Wide 0
Sidney Vianna AS9100 News PPAP in the Aerospace Sector - What is it? AS9145 - Requirements for Advanced Product Quality Planning and Production Part Approval Process AS9100, IAQG 9100, Nadcap and related Aerospace Standards and Requirements 10
H Informational What is PPAP (Production Part Approval Process)? APQP and PPAP 22
J IATF 16949 Cl. 8.4 - Externally provide process not for automotive part IATF 16949 - Automotive Quality Systems Standard 3
J Differences between a Risk Management Plan vs. Production Part Approval Process AS9100, IAQG 9100, Nadcap and related Aerospace Standards and Requirements 3
K FAI (First Article Inspection) vs PPAP (Production Part Approval Process) APQP and PPAP 15
M Interpreting Process Controls - 21 CFR Part 820.70(a) 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 5
R Identification of Russian Predicate Devices as part of the Registration Process Other Medical Device Regulations World-Wide 1
T "Special Process" Validation Requirements (21 CFR Part 820) 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 15
Marc Medical Equipment Inmetro Certification Process in Brazil - Part 2 Other Medical Device Regulations World-Wide 3
M Informational Medical Device Registration Process in Brazil - Anvisa (Part 3) Other Medical Device Regulations World-Wide 133
M Medical Device Registration Process in Brazil - Anvisa (Part 2) Other Medical Device Regulations World-Wide 71
J PPAP (Production Part Approval Process) Requirements for Annual Revalidations APQP and PPAP 1
O Outsourcing part of Design & Dev Process- Still requiring D&D ver & val-7.3.5, 7.3.6? IATF 16949 - Automotive Quality Systems Standard 6
P Hard Milling Process - Dealing with Within Part Variation for SPC Statistical Analysis Tools, Techniques and SPC 18
Q Process and Part Qualifications - Automotive Industry and Consumer Electronics IATF 16949 - Automotive Quality Systems Standard 12
S Part Marking: When in the production process to mark parts? AS9100, IAQG 9100, Nadcap and related Aerospace Standards and Requirements 9
S Marketing Process as part of QMS (Quality Management System)? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 17
E When to Validate a Process - 21 CFR Part 820.75.(a) 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 8
S Process Audit against different jobs (but part of the same process) ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 13
M Medical Equipment Inmetro Certification Process in Brazil - Part 1 Other Medical Device Regulations World-Wide 47
D Checking Rib Thickness on a Part and Necessary Process Controls Inspection, Prints (Drawings), Testing, Sampling and Related Topics 2
M PPAP (Production Part Approval Process) files for Ford APQP and PPAP 11
E APQP Process for Service Parts - Many part numbers APQP and PPAP 4
M Part & Process Approval in Medical Devices Other Medical Device and Orthopedic Related Topics 3
L Weighing plastic part to evaluate moulding process Design and Development of Products and Processes 2
Z Is Quotation a part of APQP process? APQP and PPAP 6
G Part family concept in Process FMEA - Thank You Guys! FMEA and Control Plans 2
bobdoering Statistical process control for precision machining - Part 3 - Sampling Error Imported Legacy Blogs 0
A What is PPAP (Production Part Approval Process) Why submit it and/with PSW APQP and PPAP 2
bobdoering Statistical Process Control for Precision Machining - Part 2 Imported Legacy Blogs 0
bobdoering Statistical Process Control for Precision Machining - Part 1 Imported Legacy Blogs 25
M Medical Device Registration Process in Brazil - Anvisa (Part 1) Other Medical Device Regulations World-Wide 301
B Help for beginner - PPAP (Production Part Approval Process) APQP and PPAP 9
R Is Kappa Study Required during PPAP (Production Part Approval Process)? IATF 16949 - Automotive Quality Systems Standard 9
T Production Part Approval Process (PPAP) Presentation in ppt. format APQP and PPAP 3
H What do you do when a part goes Obsolete and How do you Initiate such a Process? Document Control Systems, Procedures, Forms and Templates 7
M Audit of Goods In as part of the QSIT "Production & Process Controls" Schedule 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 4
F Who should Sign Supplier PPAP (Production Part Approval Process) documents? APQP and PPAP 13
H Who can require PPAP (Production Part Approval Process)? APQP and PPAP 7
S Tell Me All About PPAP (Production Part Approval Process) APQP and PPAP 7
P Definition Dock-to-Stock Process based on Historical Quality Performance of a Part and Supplier Definitions, Acronyms, Abbreviations and Interpretations Listed Alphabetically 8
D Source Control Drawing vs. Part Approval Process Document Control Systems, Procedures, Forms and Templates 9
S Special Process definition - Clause 7.4.1 part d AS9100, IAQG 9100, Nadcap and related Aerospace Standards and Requirements 3
ScottK Psycholgical Profile as part of the interview process? Career and Occupation Discussions 13
Z Low Process Capability - Cpk - Man-made part - What to do? Capability, Accuracy and Stability - Processes, Machines, etc. 6
Sidney Vianna Should the billing process be part of ISO 9001:2008? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 99
P Quality Manual - Process Interactions - Two part process overview map Quality Management System (QMS) Manuals 4
Similar threads


















































Top Bottom