SBS - The best value in QMS software

History - Evolution of quality in the automotive industry

M

M Greenaway

#1
#1
Has anyone got any good free literature on the evolution of quality in the automotive industry - from say the end of WWII to date ?
 
QMS for Medical Device Companies
Elsmar Forum Sponsor
Marc

Marc

Hunkered Down for the Duration with a Mask on...
Staff member
Admin
#2
#2
I think you'll have to get someone to give you an oral history. I don't recall ever seeing anything printed / on the 'net which specifically addresses the history of quality in the automotive arena. I could be wrong...
 
R

Randy Stewart

#4
#4
I have a few things from my Subsafe QAI school in the Navy. It goes back to the Thresher and Scorpion disasters (1960s) if that will help fill in some.
 
Marc

Marc

Hunkered Down for the Duration with a Mask on...
Staff member
Admin
#8
#8
Wow, Atul! That's one heck of a nice link! It pulls together a lot. I hope it doesn't disappear for a while as so many do. Thanks! :thedeal:
 
You must log in or register to reply here.
Thread starter Similar threads Forum Replies Date
M Materials/information about ISO 9001/QMS history and evolution ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 4
M Quality Manual - Where does Revision History Section go? Document Control Systems, Procedures, Forms and Templates 8
C GUDID Device record history Medical Device and FDA Regulations and Standards News 2
A Design History File - Not ready to share the design drawings or Bill of Material US Food and Drug Administration (FDA) 2
M Is There a Revision History or Change Log for Canadian Regulations? Canada Medical Device Regulations 3
C SOP unification. Revision No, Revision history Document Control Systems, Procedures, Forms and Templates 4
I Dating controlled documents after changes - Revision History Document Control Systems, Procedures, Forms and Templates 13
I Revision History Date - date of updates or date of release? ISO 13485:2016 - Medical Device Quality Management Systems 2
R No design history file or device master record ISO 13485:2016 - Medical Device Quality Management Systems 5
R Suggestions for putting together a DHF (Design History File) ISO 13485:2016 - Medical Device Quality Management Systems 3
R Implementing Design History Documents/ Technical Documents in the QMS ISO 13485:2016 - Medical Device Quality Management Systems 3
D Questions about the contents of a Design History File 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 3
bryan willemot Documenting past problem history for fasteners for AS9100 Rev D AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 2
B MDSAP 8.2.6 CH6 task 17 ANVISA 16/2013 3.2.1 - Label History in Device history record Other Medical Device Regulations World-Wide 3
R Are DMR (device master record) and DHR (device history record) inspected by FDA or audited by an NB ISO 13485:2016 - Medical Device Quality Management Systems 6
gunnyshore History of ISO 13485 ISO 13485:2016 - Medical Device Quality Management Systems 6
N Design Validation Conventions for Design History Files 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 5
Sidney Vianna Good news! Energy demand will peak for the first time in human history! Sustainability, Green Initiatives and Ecology 1
Sam Lazzara Preferred Location for Revision History Section in Documents Document Control Systems, Procedures, Forms and Templates 16
J How to document Corrections made to a Medical Device History File ISO 13485:2016 - Medical Device Quality Management Systems 1
E Updating DHF (Design History File) to include Alternative Component 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 2
M Lean Time Line (History and Theory) Lean in Manufacturing and Service Industries 5
V Template / format for Device History File & Design Verification of transdermal patch 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 1
J Electronic Device History Record (eDHR) Software Recommendations 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 1
JoCam Ownership of Design History File EU Medical Device Regulations 6
K ISO 13485 and DHF (Design History File) requirements ISO 13485:2016 - Medical Device Quality Management Systems 9
B Design history files for combination products 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 1
I Document Control - Document Revision History Question Document Control Systems, Procedures, Forms and Templates 16
K Revision History of Quality Manual Missing ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 12
M Design History File (DHF) for New Generation of Product 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 3
W Maintaining Component Traceability in DHR (Design History Record) 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 5
N 510k without DHF (Design History File) that we bought a 3 years ago US Food and Drug Administration (FDA) 4
Marc Ten City Maps from History Coffee Break and Water Cooler Discussions 0
A Medical Device Service Records linked to DHR (Design History Record)? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 2
A DHF (Design History File) for a Legacy Product (Class iii Medical Device) 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 6
B When To Share Your DHF (Design History File) With A Customer US Food and Drug Administration (FDA) 1
B Revision history for FDA's CFR 21 US Food and Drug Administration (FDA) 1
T Before recent Quality Standards - History Coffee Break and Water Cooler Discussions 11
Marc The daily routines of history's most creative minds Coffee Break and Water Cooler Discussions 1
E Better control of DHR (Design History Record) during processing Document Control Systems, Procedures, Forms and Templates 5
S Cost Targets as Design Inputs in your DHF (Design History File) US Food and Drug Administration (FDA) 7
K Explaining Gaps in Employment History Career and Occupation Discussions 56
C Should Research Findings be in the Design History File? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 1
T 510(k) Revision Level History and Submission Requirements 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 4
S Advice on moving QMS Documents and Maintaining Revision History Quality Manager and Management Related Issues 9
S MTTR - MTBF - Machine History Card template form Manufacturing and Related Processes 16
renenatasha Usage of web articles in DHF (Design History File) 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 10
R Cloud Computing Requirements for Design History Files for Software Medical Devices 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 4
Q Device History Records Maintenance - Discontinued the use of the Product 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 5
D Malfunctions, 2 year History, and Medical Device Reporting 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 1

Similar threads

Top Bottom