Customer Documents - TS 16949:2002 Clause 7.2.3.1 Interpretation

B

bibo_auto

#1
Hello Guys!
First of all let me said I think you're great. Only here there are so much information about quality matters and much more.

I would like to ask you one thing about point 7.2.3.1 from TS 16949: 2002.
Even if we are ISO/TS 16949 certified and we have all our related internal documents, sometimes our Customers asks us to use their own documents (i.e 8D report, 5 Whyanalisys, R&R etc).

The reasons for the Customer is point 7.2.3.1 but, as my understandig, this refers only to information connect to logistics and not to others documents: infact in the 16949 speaks about "..in a Customer specified language and format (e.g. computer aided design data, electronic data exchange)".

In other hands I don't understand the utility of a third part certification of our quality system (documents included) that our Customer doesn't recognize.
If the Cistomer needs some kind of documents I think they have to specified their use as a "Customer Specific requirements" and not only ask referring to the point 7.2.3.1.

Anyone as experience on this matter?

Thanks in advance.

Nicola
 
Elsmar Forum Sponsor

Jim Wynne

Leader
Admin
#2
Re: TS 16949:2002 Clause 7.2.3.1 Interpretation

Hello Guys!
First of all let me said I think you're great. Only here there are so much information about quality matters and much more.

I would like to ask you one thing about point 7.2.3.1 from TS 16949: 2002.
Even if we are ISO/TS 16949 certified and we have all our related internal documents, sometimes our Customers asks us to use their own documents (i.e 8D report, 5 Whyanalisys, R&R etc).

The reasons for the Customer is point 7.2.3.1 but, as my understandig, this refers only to information connect to logistics and not to others documents: infact in the 16949 speaks about "..in a Customer specified language and format (e.g. computer aided design data, electronic data exchange)".

In other hands I don't understand the utility of a third part certification of our quality system (documents included) that our Customer doesn't recognize.
If the Cistomer needs some kind of documents I think they have to specified their use as a "Customer Specific requirements" and not only ask referring to the point 7.2.3.1.

Anyone as experience on this matter?

Thanks in advance.

Nicola
7.2.3.1 refers primarily to electronic data transmission, but it can be broadly interpreted to refer to the "language and format" of other types of documents. If your customer expects you to use their own forms and formats for documents, it should be covered in some kind of explicit documented requirements, however. They shouldn't be allowed to use 7.2.3.1 as a substitute. Note that the clause in question says that the organization must be capable of communicating "...in a customer-specified language and format..." [emphasis added], which means that they must supply a specification for what's expected.
 
B

bibo_auto

#3
Re: TS 16949:2002 Clause 7.2.3.1 Interpretation

Thanks for the answer.

So in this case in which we don't have any requirement nor agreement with our Customer we can use our documents...
 

Jim Wynne

Leader
Admin
#4
Re: TS 16949:2002 Clause 7.2.3.1 Interpretation

Thanks for the answer.

So in this case in which we don't have any requirement nor agreement with our Customer we can use our documents...
In your original post, you indicated that "sometimes" customer ask you to use their forms. If they ask you to use their forms, you should use their forms. If they haven't asked, or specified a particular format, you should feel free to use your own.
 
Z

zancky

#5
Re: TS 16949:2002 Clause 7.2.3.1 Interpretation

hi,
from my experience I suppose the main purpose of 7.2.3.1 is to drive supplier to use the same CAD system of his customer. I.e. if Your customer is using Catia, You can tell him that Your CAD system can produce a Catia readable file but it is not true everytime. Therefore You have to buy Catia and design with it. Where I have worked once we have 4 different CAD system due to customers. More or less the same for microsoft office suite etc.
Anyway with German customers You must use their forms too (I have into my Quality System 7 different 8D forms: one is for internal use, one for customer A, even one for internal use when it is used for part of customer XXX, etc; I have declared so in my procedures and everybody are happy, customers and auditors)
 
B

bibo_auto

#6
Re: TS 16949:2002 Clause 7.2.3.1 Interpretation

Thanks Zancky.

So I understood there are differente "interpretation" about point 7.2.3.1 and people are using (expecially Customers) to give it the meaning that they wants (CAD, EDI, 8D etc)...
Even for me this point is refers to a "data" (means CAD data and EDI data) and not on the forms otherwise I can't undestrand why each organization has to develop its own documents: it would be easier to use only the documents from your Customer.
I think that the request to use Customer document has to be discussed in the revision of the contract as a "specific requirement".
If my organization has an identity and a certification, recognized by a third part body certification, with all the documents for the quality system, using others documnets it semme to me that we are loosing our identity...
Perhaps this is only my interpretation of 7.2.3.1 .... What do you think about it?
 
Z

zancky

#7
Hi Bibo,
even if we can consider 7.2.3.1 related to electronic data format, supplier must "talk" with the customer into his own language
American companies auditor check how many people actually can speak English, same for German companies, they sent 8d and e-mail in their own language.
Sometime "own language" also means to use the same forms with the same "dictionary" as they can not understand something different. As You are italian (aren't You) can You understand a problem into "vasca-dei-pesci" (english translation is "acquarium") if it is related to a car?
What about customer that ask You to fill forms only by web?
Normally they write which forms You have to use etc into the contract therefore there is nothing you can do.
Therefore my suggestion is to make a collection of all forms into Your system!

good luck
 

Raffy

Quite Involved in Discussions
#8
As far as I undertand in the requirement, On our end we ensure that we ask our customer what could be the format of the report that will be sent to them, therefore we sent these reports e.g. txt, rtf, xls, pdf. It depends what could be the specific requirement a customer need.
Raffy
 
Thread starter Similar threads Forum Replies Date
M Control of External Documents such as customer manuals AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 28
P Customer Forms as external documents Document Control Systems, Procedures, Forms and Templates 4
T Customer Specific Documents and Records - ISO 9001 Control Requirements ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 2
Q Control of Customer Documents (Documents of External Origin) AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 6
H Customer Requirements and Request for all Process Details and Documents APQP and PPAP 8
M Control of Customer Manuscripts (Manuals), Specifications - External Documents ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 11
A Before the ISO-9001 certification audit can we submit the documents to our customer ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 8
H Can the documents supplied by the client categorised as customer property?? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 6
C Customer Changes to Customer Supplied Documents - Testing Instructions US Food and Drug Administration (FDA) 2
C Control Plan - Links to Customer Documents (e.g. Print) or the Actual Specifications? FMEA and Control Plans 22
L Customer Requirements related to Retention Documents and Records period Records and Data - Quality, Legal and Other Evidence 1
A Should I use "Client" or "Customer" in my documents? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 24
P Customer Furnished Drawings Retained? Control of Documents of External Origin Records and Data - Quality, Legal and Other Evidence 4
C Controlling External Customer Documents (Documents of External Origin) Document Control Systems, Procedures, Forms and Templates 5
B Method to Ensure Latest Customer Specifications (Documents of External Origin) Customer and Company Specific Requirements 2
Sidney Vianna All the TC 176 documents - ISO 10020 - Customer Satisfaction Monitoring and Measuring ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 5
F Control Of Documents Questions - Customer Specifications / Requirements IATF 16949 - Automotive Quality Systems Standard 1
Tim Folkerts 'Quality': The Documents, System, etc. vs. 'quality': Meeting Customer Expectations Philosophy, Gurus, Innovation and Evolution 3
J Proprietary PPAP documents - Customer is also our competitor APQP and PPAP 5
Ashland78 IATF Process Control Plans not including customer name Manufacturing and Related Processes 13
T Reporting Adverse Events as Customer Complaints EU Medical Device Regulations 2
A Can a customer send a claim during PPAP? IATF 16949 - Automotive Quality Systems Standard 7
T Non-reportable customer complaints and CER EU Medical Device Regulations 2
G Customer complaint AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 22
GStough Suppliers Starting to Charge A Fee for Customer Audits Supplier Quality Assurance and other Supplier Issues 14
A Customer feedback ISO 13485:2016 - Medical Device Quality Management Systems 11
R VDA Potential Analysis - Similar product from other customer and confidentiality VDA Standards - Germany's Automotive Standards 0
B AS9100 Certification Audit Accounting for Additional Customer QMS Requirements AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 15
B IATF 16949 clause 10.2 - requirements following a customer complaint. IATF 16949 - Automotive Quality Systems Standard 9
R Customer Returns / RMA's & the need for NCR's AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 16
M 8.4.1.1 Register of approved suppliers and requirements when they are customer-designated AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 0
T Who's responsible for verification of customer specifications? IATF 16949 - Automotive Quality Systems Standard 17
D Is IATF certification required when customer doesn't require it? IATF 16949 - Automotive Quality Systems Standard 19
G Customer specific characteristics symbols Customer and Company Specific Requirements 2
S Defining special characteristics beyond customer drawing FMEA and Control Plans 11
M Customer PPm (CPPM) on Pass-Thru Items Statistical Analysis Tools, Techniques and SPC 0
V Would the customer drawing change necessitate re-PPAP of the Product? APQP and PPAP 3
S Do we have to create a new PPAP to our customer if our Sub Contractor had to change? APQP and PPAP 10
FuzzyD ISO 13485:2016 Customer Assessment OFI ISO 13485:2016 - Medical Device Quality Management Systems 2
I Restricting scope to one part number for one customer IATF 16949 - Automotive Quality Systems Standard 6
R Customer Listed on Approved Supplier List (ASL) AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 0
N 8.3.3.3 Special characteristics - Auditor said we are required to create our own, if no customer char. exist. IATF 16949 - Automotive Quality Systems Standard 10
R Audit from Customer - concerned with IP protection ISO 13485:2016 - Medical Device Quality Management Systems 4
L Documenting internal audit of customer specific requirements IATF 16949 - Automotive Quality Systems Standard 10
L Supplier Performance when your supplier is also the customer ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 17
I Customer Feedback Medical Devices ISO 13485:2016 - Medical Device Quality Management Systems 6
JoeRandom11 Question about Customer Supplied Equipment AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 2
Moncia Customer satisfaction monitoring - ISO 9001 and 14001 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 24
D Customer Survey Example - ISO 13485:2016 ISO 13485:2016 - Medical Device Quality Management Systems 7
R Customer feedbacks sampling size EU Medical Device Regulations 4

Similar threads

Top Bottom