SBS - The best value in QMS software

Should the billing process be part of ISO 9001:2008?

Should the billing/invoicing process be explicitly part of ISO 9001:2008?

  • Yes. Billing/invoicing processes should be explicitly part of the new ISO 9001

    Votes: 24 55.8%
  • No. Billing/invoicing processes should not be part of the new ISO 9001

    Votes: 19 44.2%

  • Total voters
    43
P

pinpin - 2009

#81
Just my personal opinion...

All processes need to be included as they all affect performance of our systems, either directly or indirectly, to a more or less extent.

In fact, like Production, Billing is an equal important process where our business rely on. No billing no income, poor and faulty billing process causes cash flow problem that stifles our operations. Thus, even our product quality satisfies customer, our poor management of cash flow kill us!

Rather than focusing on customer satisfaction with accuracy of our bills, we also shall look into efficiency and effectiveness of our billing process that enable us to get from external customer promptly and pay internal customers to ensure "internal customer satisfaction" and other stakeholders satisfaction.

Furthermore, some companies look into controls to prevent theft and misappropriation of fund, especially when handling cash! But many quality system folks say this is out of QMS Scope....

If we were not to do more than the "generic" requriements of ISO 9001, certification to ISO 9001 merely is a cert on the wall.:(
 
Elsmar Forum Sponsor
T

TamTom

#82
Just my personal opinion...

All processes need to be included as they all affect performance of our systems, either directly or indirectly, to a more or less extent.

In fact, like Production, Billing is an equal important process where our business rely on. No billing no income, poor and faulty billing process causes cash flow problem that stifles our operations. Thus, even our product quality satisfies customer, our poor management of cash flow kill us!

Rather than focusing on customer satisfaction with accuracy of our bills, we also shall look into efficiency and effectiveness of our billing process that enable us to get from external customer promptly and pay internal customers to ensure "internal customer satisfaction" and other stakeholders satisfaction.

Furthermore, some companies look into controls to prevent theft and misappropriation of fund, especially when handling cash! But many quality system folks say this is out of QMS Scope....

If we were not to do more than the "generic" requriements of ISO 9001, certification to ISO 9001 merely is a cert on the wall.:(

:applause: Hi,

I fully comply to this,
because altough a lot of indicators cane from the finicial departments that are used in Quality, so why don't put them in the QMS.

I vote for the Integrated Management System, that include the whole company, the depth how far I explain them could be different, but they should be included.

Greetings,

TamTom
 
W

w_grunfeld

#83
:applause: Hi,

I fully comply to this,
because altough a lot of indicators cane from the finicial departments that are used in Quality, so why don't put them in the QMS.

I vote for the Integrated Management System, that include the whole company, the depth how far I explain them could be different, but they should be included.

Greetings,

TamTom
I am probably a lonely voice here, but I don't thing the billing process is part of product realization...
I am not questioning the importance of an effective billing process but so are many other processes vital to a company's success. Should all be part of 9001?
How about accounting in general not just billing?
How about sales/marketing effectiveness?
How about auditing the CEO against some key performance targets?
Why not the whole board? Don't you think it would be beneficial to analyze past board decisions, find the root cause of bad decisions and initiate corrective actions to learn from them and reduce the probability of future bad decisions? There is no end to it....
 

Sidney Vianna

Post Responsibly
Staff member
Admin
#84
I am not questioning the importance of an effective billing process but so are many other processes vital to a company's success. Should all be part of 9001?
As I (tried to) explained when I started the thread: ISO 9001 is about customer satisfaction. Very few processes can impact customer satisfaction as much as the billing process.

ISO 9001 attempts to provide a model for managing a subset of an organization's business system. Customer satisfaction will always be affected by a supplier's billing process.
 
Q

qualityboi

#85
Hi Sidney,

What metrics would you use for customer satisfaction out of the billing process?
Complaints due to billing? Bill to Quote accuracy?

TIA
 
D

Desara01

#86
Ok - I voted yes but the reality is - who cares whether it's an ISO requirement or not? What's the right thing to do for your customer? Customer-facing processes should be part of your quality/business system (why do people continue to say these are two separate things??)

I conduct Voice of the Customer interviews with - er - customers. Several customers have made comments about the invoicing process which would never have shown up on a financial audit. For example - issuing an invoice for 16 cents. Technically the invoice is correct - but it cost us more to produce the invoice, and for the customer to pay it, than it was actually worth.

It's not just about meeting GAPs, it's about what it's like to do business with your company. Make it easy for your customers to do business with you, and they will remain customers. :bigwave:
 
W

w_grunfeld

#89
ISO 9001 is a standard. It is about what it says it is. Standards are written so that everybody does what it says they should be doing. It doesn't say anywhere that you can't do other things-it's just not part of the standard.
The TC 176(?) comittee that is responsible for the standard may welcome your ideas of what other things should be made part of the standard, or they might reject it.
But I don't think we as quality practitioners should read into it what's not stated.
If it were say.. a communication standard...would you sugest adding an extra bit of data because from your experience it would improve the standard? Obviously not, in my opinion quality practitioners should be the last people to interpret standards acoording to their personal likes/preferences.
 

Jim Wynne

Staff member
Admin
#90
ISO 9001 is a standard. It is about what it says it is. Standards are written so that everybody does what it says they should be doing. It doesn't say anywhere that you can't do other things-it's just not part of the standard.
Then you advocate not doing anything that's not specifically called for in the standard?
 
Thread starter Similar threads Forum Replies Date
A Should we assign the PRRC before the date of application of MDR (26 May 2021)? EU Medical Device Regulations 0
J UDI-DI how should we interpret Device version or model to determine if a new UDI-DI is needed? EU Medical Device Regulations 0
Sidney Vianna Interesting Discussion Should ISO 9004 be changed from a guidance document to a requirements standard? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 7
A Should I take an online course for a career in Occupational Health and Safety? Career and Occupation Discussions 2
J Should a Class 1 medical device with an option to measure body weight be considered Class 1m? EU Medical Device Regulations 0
K Should APQP/PPAP has its own section in a QM? Quality Management System (QMS) Manuals 1
S What should i choose for "testing procedure" characteristics? (N95) General Information Resources 0
P Should eIFU link per ISO 15223-1:2016 be added to labels out of scope of Reg 207/2012? EU Medical Device Regulations 1
S Which Sampling Plan(s) Should I Use? Inspection, Prints (Drawings), Testing, Sampling and Related Topics 7
A Document release vs its related training. Which should come first? ISO 13485:2016 - Medical Device Quality Management Systems 18
S Which department should prepare the control plan? could you show me a standard regarding to this matter. FMEA and Control Plans 17
J Help settle a disagreement: Should external providers of preventive maintenance be on your ASL? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 5
N Master Samples - What should we be keeping? IATF 16949 - Automotive Quality Systems Standard 9
G Supplier delivered recent PPAP, should he deliver yearly layout inspection? IATF 16949 - Automotive Quality Systems Standard 4
John Broomfield Vote - Should ISO9004 Become a Requirements Standard? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 11
A Capability Study - in the beginning of your career what should you have known about the tool Quality Tools, Improvement and Analysis 11
J Should Loading and Unloading be Included in Cycle Times? Lean in Manufacturing and Service Industries 14
E Manufacturers should develop a testing device for covid19 Service Industry Specific Topics 0
T 510(k) submission - Which name should I use in the submission? Other US Medical Device Regulations 3
N ISO 19011:2018 - 5.4.2 "...audit program should engage in appropriate continual development..." Training - Internal, External, Online and Distance Learning 4
G Should I perform Gage R&R only at the beginning of a new project? Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 6
DuncanGibbons Should the requirements FAA/EASA Part 21 be addressed within the QMS and AS9100D quality manual? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 5
M Should 510(k) Predicates be Actively Listed Devices? Other US Medical Device Regulations 12
B Why the Greek god Hephaestus should have done a design FMEA (DFMEA) on his giant robot APQP and PPAP 1
J On PFMEA for danger labels - Label always should be assigned severity 10 ? FMEA and Control Plans 3
H Who should be listed as the manufacturer/distributor on the box? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 15
M MDR, RED and LVD - Should our device comply with them? EU Medical Device Regulations 3
BeaBea How Many Processes should be created for each Department? Process Maps, Process Mapping and Turtle Diagrams 5
M Should volume of sales be factored into risk probability assessments? ISO 14971 - Medical Device Risk Management 33
MrTetris Should potential bugs be considered in software risk analysis? ISO 14971 - Medical Device Risk Management 5
S Should safety checks be included in the Control Plan? IATF 16949 - Automotive Quality Systems Standard 5
M Which incubation condition should be selected to recover both bacteria and fungus effectively Miscellaneous Environmental Standards and EMS Related Discussions 3
D Is there a specific location for PPE such as safety glass holders and glove dispensers should be mounted Occupational Health & Safety Management Standards 10
Robert Stanley Which Registrar Should I Choose for ISO 9001:2015 registration? Registrars and Notified Bodies 10
M Who should receive the bills from suppliers and vendors, account payable or procurement? Consultants and Consulting 4
V IATF 16949 8.4.1 Control of externally provided processes, products and services - Should the CB be on our Approved Supplier List? IATF 16949 - Automotive Quality Systems Standard 10
A We are ISO 13485:2016 should we be audited to ISO 14971 ISO 13485:2016 - Medical Device Quality Management Systems 16
E Received a Major finding during IATF Surveillance audit for loss of BIQS Level 3 (more than 6 SPPS in 6 months)...how should we address SYSTEMIC CA? IATF 16949 - Automotive Quality Systems Standard 11
J Organization merger. Should we keep two separate ISO 13485 certificates? ISO 13485:2016 - Medical Device Quality Management Systems 6
S Companies that maintain your machine should be in ASL? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 2
S Use of "Shall" versus "Should" in Procedures ISO 13485:2016 - Medical Device Quality Management Systems 26
D Class II medical device - When should a complaint be closed? Customer Complaints 6
Sidney Vianna IATF 16949 News Presentations from the latest IATF Stakeholder Event - Expectation that IATF 16949 certification should equate with product quality. Misguided? IATF 16949 - Automotive Quality Systems Standard 7
L Clause 0.4 of ISO 9001 and EHS - Where should I stop the inclusion of EHS in my QMS ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 8
Ed Panek Part 11 Self Certify Memo - What else should it cover? Qualification and Validation (including 21 CFR Part 11) 5
H Should I mention machine/Equipment password In SOP? Qualification and Validation (including 21 CFR Part 11) 4
D How long should we keep the spare parts available for our medical device, after we have stopped the production? ISO 13485:2016 - Medical Device Quality Management Systems 0
H Statistical Techniques Procedure - What should be included Document Control Systems, Procedures, Forms and Templates 4
Q How should I analyze measurement correlation between me and customer? Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 12
Sidney Vianna Interesting Discussion ISO 9001:2024 - What should be changed in the next Edition of ISO 9001? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 114

Similar threads

Top Bottom