Technical automotive metal stamping cliffnotes needed!

T

TROQC

Starting to get Involved
#1
#1
Can anyone recommend a class or book that can help with technical understanding or vocabulary for someone new to quality who can write well, but is completely new to automotive metal stamping?
 
Paper to QMS ad
Elsmar Forum Sponsor
G

Golfman25

Trusted Information Resource
#3
#3
What type of issues are you having? Ask away.

Check SME.org. Search metal stamping in their bookstore.

Get metalforming magazine from PMA.org

And stamping journal from fmanet.org
 
T

TROQC

Starting to get Involved
#5
#5
These are great suggestions... Thanks. The goal is to be able to speak fluently when I'm describing an issue, and have a general comprehension of what is being described by "lifers" in this industry. I, of course, was promised training when I was hired, & have been given some, but not nearly what I feel I need.
 
You must log in or register to reply here.
Thread starter Similar threads Forum Replies Date
DuncanGibbons Technical Data Package vs Digital Product Definition APQP and PPAP 0
D Hospital Decontamination and the MDR - Technical Files, UDI and PMS EU Medical Device Regulations 3
F Software as a Medical Device (SaMD) Technical File Requirements Manufacturing and Related Processes 1
S Technical File for Surgical Mask in Class 1 MDD Elsmar Cove Forum ToS and Forum Policies 1
A Technical File - Updating Applied Standards EU Medical Device Regulations 4
M What to be careful about/focus on when doing a Technical File review EU Medical Device Regulations 4
Watchcat Anyone had an MDR technical file review/audit yet? EU Medical Device Regulations 13
G Same intended use devices - Technical file EU Medical Device Regulations 2
I Maintaining Technical Documentation under MDD and MDR EU Medical Device Regulations 1
M Basic UDI and technical documentation EU Medical Device Regulations 1
B Clause 5.1.12 of Technical Standard IEC 62304/A1 IEC 62304 - Medical Device Software Life Cycle Processes 5
V Iso13485 certification vs CE technical audit ISO 13485:2016 - Medical Device Quality Management Systems 3
F Management of Software version while NB reviews Technical file CE Marking (Conformité Européene) / CB Scheme 7
D Risk Analysis & Technical File - What detail goes in the Risk Management Report ISO 14971 - Medical Device Risk Management 5
F Recommended practice for furnishing Technical Procedures ISO 17025 related Discussions 1
S How to find technical specification for facilities maintainance ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 2
L Special Processes - Technical reason concerning torque - Anaerobic compounds Manufacturing and Related Processes 10
N Technical file requirements class 1 device MDR Other Medical Device Regulations World-Wide 6
R Implementing Design History Documents/ Technical Documents in the QMS ISO 13485:2016 - Medical Device Quality Management Systems 3
T Change in BRH (Brazilian Registration Holder) Technical Manager Other Medical Device Regulations World-Wide 2
C Maintenance of Product Technical Documentation EU Medical Device Regulations 3
O Medical Device Technical File Confidentiality - On site reviews EU Medical Device Regulations 14
N How to Write and Compile a Technical File for CE Marking CE Marking (Conformité Européene) / CB Scheme 4
N Technical File Reviewer has requested more testing to ISO 10993 Other Medical Device Related Standards 10
M Informational USFDA draft guidance – Technical Performance Assessment of Quantitative Imaging in Device Premarket Submissions Medical Device and FDA Regulations and Standards News 0
M Informational USFDA draft guidance – Technical Considerations for Non- Clinical Assessment of Medical Devices containing Nitinol Medical Device and FDA Regulations and Standards News 0
C Access to Technical Documentation - MDR Chapter VI Article 61 EU Medical Device Regulations 4
M Technical File (STED) labelling - When you compile tech files do we have to include all the product labels? EU Medical Device Regulations 2
M Informational IMDRF final document – Assembly and Technical Guide for IMDRF Table of Contents Submissions Medical Device and FDA Regulations and Standards News 4
N EU MDR Basic UDI-DI and Technical Documentation for Systems EU Medical Device Regulations 22
M Medical Devices and ASD-STE100 (Simplified Technical English) Other Medical Device Related Standards 0
B IATF 16949:2016 – Technical Specification (eBook edition) IATF 16949 - Automotive Quality Systems Standard 1
S MDR Technical File Structure Requirements EU Medical Device Regulations 12
L 510k exemption process - Do you still need to submit technical dossier? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 5
D MDD to MDR - Technical File conversion EU Medical Device Regulations 4
J Connection between Technical File and Declaration of Conformity CE Marking (Conformité Européene) / CB Scheme 2
I MDD Class I software technical documentation sample EU Medical Device Regulations 2
M Annex II - Technical Documentation. V&V, Performance and Safety EU Medical Device Regulations 3
TechnicalGuy Technical File Review - Transfer to a new NB EU Medical Device Regulations 3
J Brazil - Submitting Technical Files Other Medical Device Regulations World-Wide 2
A CTD (Common Technical Document) for a Topical Preparation Pharmaceuticals (21 CFR Part 210, 21 CFR Part 211 and related Regulations) 2
J One Medical Device, two indications, two classes, one technical file? EU Medical Device Regulations 3
S. Moore Technical or Systemic cause for 8D Nonconformance and Corrective Action 7
Q New Casting Supplier System Assessment - What technical questions to ask? Supplier Quality Assurance and other Supplier Issues 3
A Technical file requirement for Class IIb medical device CE Marking (Conformité Européene) / CB Scheme 3
D Technical file structure/content requirements for Class IIa devices & new MDR EU Medical Device Regulations 14
J Update Technical File for EU Class IIa Medical Software Products EU Medical Device Regulations 3
D MDR and Summary Technical Documentation Files EU Medical Device Regulations 13
B Gap analysis of new start-up company technical documentation CE Marking (Conformité Européene) / CB Scheme 1
T IVD - Self Declaration - Technical File - Template wanted Various Other Specifications, Standards, and related Requirements 9

Similar threads

Top Bottom