Substance reporting for PPAP GMW 3059

L

Laura M

#11
You'd kindof expect it to be in the Additional Customer requirements section of QS. I haven't been with a Tier 1 since March '99, but had no info on it before I left. I'll call my old colleagues and see what they know.
 
Elsmar Forum Sponsor

Marc

Hunkered Down for the Duration with a Mask on...
Staff member
Admin
#13
I have 19 files with the extension .fxr that were e-mailed to me. I'll post them in the pdf_files directory, but I have no idea what program will read the files.
 
B

billsfan

#14
Marc,
I just sent you a 21 page fax.
I'll keep my fingers crossed!
Hope it comes through O.K.
If not, I could mail you a copy.
By the time we get copies distributed,
GM will change the spec!
Later dudes....
 

Marc

Hunkered Down for the Duration with a Mask on...
Staff member
Admin
#15
The FAX came through fine, but I really can't post it. The Winfax files are posted in the pdf_files directory - I expect anyone with Winfax can download them and open them.

To make things real simple, where did you get the copy (original?) you have?
 
B

billsfan

#16
Marc,
I got my copy from Joyce Sheffield, PPAP Coordinator, Purchasing - Supplier Quality.
(Delphi-E Anderson,In.)
If you can get fax numbers for everyone that would like a copy, I would be happy to fax copies to everyone.
Let me know if I can be of help.
 

Marc

Hunkered Down for the Duration with a Mask on...
Staff member
Admin
#17
The best way to answer is to say:

Everyone who wants a copy --> leave a FAX number!

Secondarily, if you have a phone number for the gal you got your copy from, folks can call and get an original, no?
 
B

billsfan

#18
Marc,
Thanks for the advise.
I checked with my Delpi contact, she said they had some difficulty making the GMW 3059 available electronically, so they sent copies out via mail. She advised that you check with your SQA at Delphi-E for a copy.
I am willing to fax copies to all that provide a fax number. Or my Delphi contact has offered the same. I must warn you, it's 21 pages (with my cover sheet.)
My contact;
Joyce Sheffield
PPAP Coordinator
Purchasing - Supplier Quality
Plt. 18 Rm. 115
2900 Scatterfield Road
Anderson, In 46013
Tel: (765) 646-2581
Fax: (765) 646-3974
 
M

Mike Murphy

#19
"I am willing to fax copies to all that provide a fax number." (billsfan)

I'm not going to refuse.
Here is my fax number: 864-457-7111

Marc. Got the files from the pdf directory and as anticipated I had some difficulty opening the files but I have not given up yet. I will open them, even if it.....
OK., let me calm down now.

Talk later.

Thanks dudes.
 
L

Laura M

#20
I just heard from my Delphi contacts that the GM1000 is still being used, with the other form released, but not required until 2003 MY parts? Something about the reportable materials requirements change, relative to the products they produce? (The person I talked to didn't have the whole scoop other than they didn't need to do it yet) Maybe the government requirements on what requires reporting are changing and thats when this form needs to be used. I should be able to get a copy of the procedure and form, but I don't think they'll be electronic.
 
Thread starter Similar threads Forum Replies Date
M Medical device substance based-leachables Other Medical Device Related Standards 2
M Europe GMP medical devices - Combination products - Ancillary medicinal substance CE Marking (Conformité Européene) / CB Scheme 4
M ISO 10993-17 - Ancillary Medicinal substance leachables Medical Device and FDA Regulations and Standards News 1
K Contains hazardous substance symbol EU Medical Device Regulations 1
A Teamcenter Substance Module RoHS, REACH, ELV, IMDS and Restricted Substances 0
D Substance of concern (SOC) management procedure wanted Reliability Analysis - Predictions, Testing and Standards 3
C Substance based Medical Device Classification under MDR - Rule 21 EU Medical Device Regulations 9
S Compliance to GADSL (Global Automotive Declarable Substance List) RoHS, REACH, ELV, IMDS and Restricted Substances 4
B Mitigation of emission of flames, molten metal, poisonous or ignitable substance IEC 60601 - Medical Electrical Equipment Safety Standards Series 2
P Dimethylnitrosoamine CAS:62-75-9 as prohibited substance acc. GADSL RoHS, REACH, ELV, IMDS and Restricted Substances 5
W REACH - Candidate List Substance vs. Authorisation List Substance in EEE RoHS, REACH, ELV, IMDS and Restricted Substances 1
T Mercury is covered under RoHS but is not a substance of very high concern (SVHC) ? RoHS, REACH, ELV, IMDS and Restricted Substances 2
Q Restricted Substance in my Product - How to declare problem? RoHS, REACH, ELV, IMDS and Restricted Substances 3
Q SVHC (Substance of Very High Concern) Declaration for Packaging Material RoHS, REACH, ELV, IMDS and Restricted Substances 1
Kales Veggie Ford RSMS (Restricted Substance Management System) 2008 released / GADSL categories RoHS, REACH, ELV, IMDS and Restricted Substances 16
Kales Veggie Global Automotive Declarable Substance List (GADSL) 2009 released..... Miscellaneous Environmental Standards and EMS Related Discussions 2
M How To Include Substance of Concern (SOC) Free Into TS16949 Internal Audit Plan IATF 16949 - Automotive Quality Systems Standard 1
Z 'Duty to Declare' substance - Is submission of IMDS sufficient? RoHS, REACH, ELV, IMDS and Restricted Substances 2
E The EU regulation for 'Restriction of hazard substance' (RoHS)? RoHS, REACH, ELV, IMDS and Restricted Substances 5
G Trying to find CAS numbers - The Database of chemical substance information IATF 16949 - Automotive Quality Systems Standard 3
S Is Toluene (Methylbenzene) a banned or restricted substance Miscellaneous Environmental Standards and EMS Related Discussions 4
N Incoming Product Quality - Receiving inspection for chemical substance Inspection, Prints (Drawings), Testing, Sampling and Related Topics 3
S Reporting REACH - Electronic components distributor REACH and RoHS Conversations 5
A OQ and reporting issues Qualification and Validation (including 21 CFR Part 11) 2
R Vigilance reporting to the country of the EU authorised representative EU Medical Device Regulations 2
M Is it Necessary to Use Health Canada Form when Reporting? Canada Medical Device Regulations 1
L Proof of Concept Studies - Do we need to comply with SAE reporting? Medical Device and FDA Regulations and Standards News 3
G ISO 17025-2017 Management Review reporting items - Inputs ISO 17025 related Discussions 1
A Medical device Reporting : Good Faith Effort for Additional information Other US Medical Device Regulations 2
B FDA-Medical Device Reporting (MDR )procedure compliant with 21CFR section 803 US Food and Drug Administration (FDA) 0
F Risk for Quality Assurance Department in a Hospital - Hospital Incident Reporting ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 7
M Differences in post market safety reporting for Combination Product Applicants Medical Device and FDA Regulations and Standards News 1
F ISO 13485 8.2.3 Reporting to regulatory authorities: Question regarding a procedure for this clause. ISO 13485:2016 - Medical Device Quality Management Systems 4
L Adverse Event Reporting New Zealand Other Medical Device Regulations World-Wide 11
M Informational New Zealand – Changes to Medical Device Adverse Event Reporting process Medical Device and FDA Regulations and Standards News 0
K Reporting a Change of Contract Manufacturer for a 510(k) cleared device Other US Medical Device Regulations 5
MDD_QNA How to deal with FDA after not reporting anything for several years Other US Medical Device Regulations 14
D Accident reporting categories Occupational Health & Safety Management Standards 1
T Trend Reporting under the EU MDR EU Medical Device Regulations 12
M Informational TGA – Medical device incident reporting (MDIR) guide Medical Device and FDA Regulations and Standards News 0
M Informational US FDA Final guidance – Postmarketing Safety Reporting for Combination Products Medical Device and FDA Regulations and Standards News 0
M Informational IMDRF proposed document – IMDRF terminologies for categorized Adverse Event Reporting (AER): terms, terminology structure and codes (Edition 4) – Anne Medical Device and FDA Regulations and Standards News 0
M Informational Health Canada – Mandatory reporting requirements for hospitals Medical Device and FDA Regulations and Standards News 0
M Informational US FDA – Statement on agency’s efforts to increase transparency in medical device reporting Medical Device and FDA Regulations and Standards News 0
A Japan's Requirements for Reporting Medical Device Adverse Events Other Medical Device Regulations World-Wide 2
T Why do most companies have Quality reporting to Engineering or Operations and not to CEO? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 45
M Informational TGA – Medical device annual reporting – Sponsor obligations Medical Device and FDA Regulations and Standards News 0
Marc European universities dismal at reporting results of clinical trials - 2019 Other Medical Device Regulations World-Wide 0
W SOP for Vigilance reporting covering multiple requirements Document Control Systems, Procedures, Forms and Templates 3
M (How To) Getting Data From Vision Machine To Reporting Software Misc. Quality Assurance and Business Systems Related Topics 0

Similar threads

Top Bottom