How do you comply with 7.2.3 Customer Comunication

Michael_M

Trusted Information Resource
I have a question regarding 7.2.3 Customer Communication.

Do you have a formal system to track this?

What method do you use to track this?

What do you actually track?



Background information: We are a production machine shop that manufactures parts to customer supplied requirements. We do no design or development. About 90% of all customer communications is through e-mail but sometimes customers call with inquiries about delivery times, changing delivery times, asking for quotes to be completed, etc.

Our procedure indicates that we will track all customer communications and this needs to be changed but I am not sure how and am looking for ideas.

Right now the main person responsible is not doing much other than keeping track of the e-mails. As this technically violates our procedure (we say 'all') we need to address this. The person responsible would prefer not to have to track communications but is willing to if required, we just are not aware enough to know what we should actually track. I want something that will help the company and will conform to AS9100 requirements.

If you can tell me how you track customer communications, how you use it, and when, I would be grateful.
 

John Broomfield

Leader
Super Moderator
Re: Question regarding 7.2.3 Customer Comunication

Michael,

Comms that relate directly to a customer are kept by the person responsible for that customer in the folder with the customer's name.

Actions taken to close inquiries, requests, changes, compliments and complaints are recorded either on the document itself or on a log. Appended notes are dated and record the action taken and by whom.

Emails are converted to .pdf before filing so they can then be searched, found and marked up with actions taken, by whom and when.

Folders are on the network accessible by all authorized users. Their location and other controls are specified in the documented filing and archiving procedure so any authorized person can immediately see the status and reliably inform the customer by looking at the electronic file. Indeed, this is the objective.

John
 
P

PaulJSmith

Re: Question regarding 7.2.3 Customer Comunication

We use a customer relationship management (CRM) software called GoldMine, which helps us track all of our contact with our customers.
 
R

Reg Morrison

Our procedure indicates that we will track all customer communications and this needs to be changed but I am not sure how .
Did a consultant help you? Customer communication does not require a documented procedure. And, why would you self enforce a requirement of TRACKING communications?

Pay close attention to what the standard requires and don't create a bureaucratic nightmare of TRACKING anything. Folders in email management software allow for that. Not all verbal communication will have to be recorded. When more and more "non conventional" modes of communication are used, such as text messages, whatsapp, etc. you could be in a world of hurt if you self require to track communication with customers when the standard doesn't.
 

Big Jim

Admin
Did a consultant help you? Customer communication does not require a documented procedure. And, why would you self enforce a requirement of TRACKING communications?

Pay close attention to what the standard requires and don't create a bureaucratic nightmare of TRACKING anything. Folders in email management software allow for that. Not all verbal communication will have to be recorded. When more and more "non conventional" modes of communication are used, such as text messages, whatsapp, etc. you could be in a world of hurt if you self require to track communication with customers when the standard doesn't.

I agree with this.

Basically the standard says that you will have channels of communication available so that customers can communicate with you.

An auditor can easily confirm that by noticing that you have a working phone system and that you frequently receive orders and so on by email.

When documents and records are not required and the organization has not chosen to include the need for any topic such as the one at hand, auditors need to determine what your practice is by interviewing and observing.

This one is easy to confirm by interview and observation.
 
M

Moonlight17

Hi Michael,
As with many of the posters before, we track communications with customers during daily activities:
Account managers use a CRM software to record quotes, tenders, contracts, changes.....
Customer Services use a tracking software to record requests, complaints, querys, thanks........
We don't have a documented procedure for this, it is part of the initial training when a member of staff joins these departments and can be observed by auditors (internal & external) to prove we communicate with the customer.
 
R

Reg Morrison

Yes a consultant is helping us. Is this a common issue with consultants?
Unfortunately, SOME consultants develop processes and procedures that are much more complex and bureaucratic than needed, in order to "justify" the time they are charging. As I said, in my previous post, there is no requirement in the standard for you to TRACK communications. Of course you do want to have an effective system that allows you to manage the communication exchanges you have with the customers, but any decent email management application can facilitate that.

For some organizations, having a sophisticated tracking capability might be worthy, but for the average machine shop, it seems to be a bureaucracy that would not provide a return on the investment.
 

Big Jim

Admin
Unfortunately, SOME consultants develop processes and procedures that are much more complex and bureaucratic than needed, in order to "justify" the time they are charging. As I said, in my previous post, there is no requirement in the standard for you to TRACK communications. Of course you do want to have an effective system that allows you to manage the communication exchanges you have with the customers, but any decent email management application can facilitate that.

For some organizations, having a sophisticated tracking capability might be worthy, but for the average machine shop, it seems to be a bureaucracy that would not provide a return on the investment.

Related to that is that many consultants really only have one package that they try to make "one size fits all". A good consultant will taylor things to better fit each company.

This can be so bad that I sometimes see an ISO 9001 manual that includes provisions for MANY AS9100 requirements, including sometimes forgetting to change AS9100 to ISO 9001.
 
Thread starter Similar threads Forum Replies Date
J WAIVED ON Q1 - We Don't have to comply with FORDS customer specific requirements IATF 16949 - Automotive Quality Systems Standard 3
J How should customer complaints be handled to comply with ISO 9001? Customer Complaints 4
J How to comply with 7.2.1 - Customer Related Process ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 6
R TS 16949 Clause 5.5.2.1 Customer Representative - What do you do to comply? IATF 16949 - Automotive Quality Systems Standard 15
Q Comply with 17025 or Customer? ISO 17025 related Discussions 6
R Can an organization be ISO certified if it doesn't comply with each clause? ISO 13485:2016 - Medical Device Quality Management Systems 1
D What does a contract manufacturer have to do to comply with for MDR? EU Medical Device Regulations 2
I Certificate of Conformity to NFL 00-015 How Do We Comply? Document Control Systems, Procedures, Forms and Templates 0
T Non API products need to comply to API Q1? Oil and Gas Industry Standards and Regulations 3
F Labelling to comply with both FDA and MDR US Food and Drug Administration (FDA) 6
M FULFILMENT of compliance obligation versus COMPLY with compliance obligations ISO 14001:2015 Specific Discussions 2
L Proof of Concept Studies - Do we need to comply with SAE reporting? Medical Device and FDA Regulations and Standards News 3
M MDR, RED and LVD - Should our device comply with them? EU Medical Device Regulations 3
R MDR standards - which standards to comply with ? EU Medical Device Regulations 3
M Informational Some things the EU MDR 2017/745 does not tell you, but you may need to know to comply with it effectively – Part 1 Medical Device and FDA Regulations and Standards News 0
B How to comply with IATF 16949:2016 9.3.2.1k - Management review IATF 16949 - Automotive Quality Systems Standard 2
S How to make Single Sign On (SSO) Comply e-sig requirements? ISO 13485:2016 - Medical Device Quality Management Systems 4
Z Does a website needs to comply with Part 11? Qualification and Validation (including 21 CFR Part 11) 6
Q How to comply with ISO 9001:2015 Clause 7.4 Communication ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 3
B Quality Policy does not include a commitment to comply with legal requirements Quality Management System (QMS) Manuals 32
S A CE Marked Product that does not comply with the Standard EU Medical Device Regulations 7
H Job Descriptions to comply with ISO Standards ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 10
M Medical devices are CE mark but not sold in EU - Need to comply with REACH? RoHS, REACH, ELV, IMDS and Restricted Substances 9
M Do I need to comply with both the MDD and the PED for my Medical Device? EU Medical Device Regulations 8
S Selecting materials for implants to comply with ISO 10993 biocompatibility Other Medical Device Related Standards 4
A Type of Materials to comply with IEC 60601 (Dental Laser Case) IEC 60601 - Medical Electrical Equipment Safety Standards Series 2
S Definition Comply - What does 'comply' mean to you? (Definition) Definitions, Acronyms, Abbreviations and Interpretations Listed Alphabetically 3
O Comply with 21 CFR 11, but no other FDA regulations? Qualification and Validation (including 21 CFR Part 11) 4
J ISO 9001 Clause 7.5.2 Validation of Processes - How to comply? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 32
A ISO/TS 16949 - Comply SPC requirements Statistical Analysis Tools, Techniques and SPC 22
K Identifying Required Testing to comply with IEC 60601 EU Medical Device Regulations 4
G What is meant by FAI (First Article Inspection) and how do we comply? AS9102 AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 26
C Do all Class 1 Medical Devices (Electrical) have to comply with IEC60601-1? IEC 60601 - Medical Electrical Equipment Safety Standards Series 11
P Outsourced Manufacturing - Making Subcontractors comply with TL9000 TL 9000 Telecommunications Standard and QuEST 2
R Dielectric Strength of Triple Insulated Wire to comply with 2MOPP IEC 60601 - Medical Electrical Equipment Safety Standards Series 3
Fender1 How to comply with ISO 9001 and provide quick/short lead-time orders? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 13
B Commitment to Comply - ISO 14001 Clause 4.2 - Environmental Policy ISO 14001:2015 Specific Discussions 6
gdwaikle Are Component Manufacturers required to comply with ISO13485:2003 ISO 13485:2016 - Medical Device Quality Management Systems 4
G How to comply with 4.4.5 Contol of Documents - Documents of External Origion Miscellaneous Environmental Standards and EMS Related Discussions 6
J Which kind of medical equipment must comply with IEC60601-1-8? IEC 60601 - Medical Electrical Equipment Safety Standards Series 2
A Procedure for Translating User Documentation to comply with MEDDEV 2.5/5 Other Medical Device Regulations World-Wide 14
H Proprietary Processes - How to Protect and still comply when performing an FAI? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 5
D How To Comply with ISO 9001 Clause 6.2.2 d (Personnel Awareness) ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 16
P ISO 14971 - Is it a guidance document or should we fully comply with it? ISO 14971 - Medical Device Risk Management 14
J Does my company's Business Plan Contents comply with requirements of TS 16949? IATF 16949 - Automotive Quality Systems Standard 2
AnaMariaVR2 Link between failure to comply w/ Lab PPE standards & ISO9001 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 4
harrysons Automotive product transferring process what requirement to comply? IATF 16949 - Automotive Quality Systems Standard 3
A How to comply with ISO/IEC 17025 Laboratory Requirements ISO 17025 related Discussions 7
L Questions: Plastic Food Container to comply with FDA US Food and Drug Administration (FDA) 6
Q Product Realization Procedure - How to comply with ISO 9001 Clause 7.1 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 9

Similar threads

Top Bottom