SBS - The best value in QMS software

Advantage between ISO 9001:2000 vs ISO 9001:2008

M

mohammedrenu

#1
Dear All

Could please share your comments for Advantage of ISO 9001:2000 to ISO 9001:2008 standard.

Thanks well in advance

BR
 
Elsmar Forum Sponsor
S

samsung

#2
Re: Advantage in between ISO 9001:2000 vs 2008

Dear All

Could please share your comments for Advantage of ISO 9001:2000 to ISO 9001:2008 standard.

Thanks well in advance

BR
Are you concerned about the changes/comparison between the two versions? If so, please refer to the attachment in post#35 in this thread.
 
M

mohammedrenu

#3
Re: Advantage in between ISO 9001:2000 vs 2008

Thanks!

But i want to know ISO 9001:2008 advantage comparing to 2000 and what benefit gets when company upgrade the system in 2008.

Its general discussion for better understanding

BR
 

somashekar

Staff member
Super Moderator
#4
Re: Advantage in between ISO 9001:2000 vs 2008

Thanks!

But i want to know ISO 9001:2008 advantage comparing to 2000 and what benefit gets when company upgrade the system in 2008.

Its general discussion for better understanding

BR
First is that the ISO 9001:2000 is no more the current version and so, to be certified to ISO 9001, it must now be to the 2008 version. The cutoff date is now past.
And last is that, if you have applied the ISO 9001:2000 sincerely and with purpose, you have nothing much to do. Else its an opportunity to take a step ahead on continual improvement.
 
Last edited:
#6
Dear All

Could please share your comments for Advantage of ISO 9001:2000 to ISO 9001:2008 standard.

Thanks well in advance

BR
As has been said, there's no practical difference. However, if an organization went from ISO 9001/2 to ISO 9001:2000, without using the 'process approach' then the 'upgrade' opportunity will benefit the organization if they take the time to re-evaluate the QMS they have. So, it's not the standard, but through Management Review, critically review the QMS and see if you truly meet ISO 9001:2008...
 
#9
Thank you all, i communicate to client regarding this.

BR
What is your role in communicating this information to a client? Are you acting as a consultant, for example? Doesn't the client have a copy of the 2008 version? If they are already registered, shouldn't they be in process with their 2008 certificate?
 
Thread starter Similar threads Forum Replies Date
Wes Bucey Inspection - Done right, it can be a marketing advantage Manufacturing and Related Processes 3
J What is the advantage of having an NCA 3800 Quality Certificate Various Other Specifications, Standards, and related Requirements 3
C Advantage of an XR chart vs. Runchart Quality Assurance and Compliance Software Tools and Solutions 4
Q 510k for Exempt Class I Medical Device - Industry Advantage to having a 510k Approval 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 12
J Advantage of having 2 marks - RvA and ANAB, for example Registrars and Notified Bodies 5
Ajit Basrur Environmental Advantage of our Organization - Power Point .ppt presentation needed Miscellaneous Environmental Standards and EMS Related Discussions 3
M What is the advantage of ISO? Private school that teaches from KG to grade 12 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 12
Moumen H Variations between ASTM A29 Standard for steel bars and Mill test certificates specs Manufacturing and Related Processes 1
N R&R for Differences between 2 measurements Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 4
S Distinction between a critical supplier and a Virtual manufacturer EU Medical Device Regulations 2
I Сorrespondence between hazards and risks ISO 14971 - Medical Device Risk Management 2
W What is the difference between TYPE B and TYPE BF? IEC 60601 - Medical Electrical Equipment Safety Standards Series 2
T The difference between ISO 14644-3:2005 and ISO 14644:2019 Other Medical Device Related Standards 2
Q Terminal Lugs sizes - Difference between 225/24 vs. 275/24 lugs Manufacturing and Related Processes 2
T Relationship between ISO 9001 and ISO – IEC BS EN 870079- 34 2020 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 5
M Difference between "Production Trial Run" and "Run at Rate" IATF 16949 - Automotive Quality Systems Standard 8
Ron Rompen Surface Finish Correlation between Ra, Rz and Tp (bearing surface ratio) General Measurement Device and Calibration Topics 3
L MRA between EU and Switzerland - 1/2021 EU Medical Device Regulations 2
D Difference between Test Method Validation and Gage R&R Qualification and Validation (including 21 CFR Part 11) 18
K Joint approval between OEM and Manufacturer on Design Documents ISO 13485:2016 - Medical Device Quality Management Systems 4
C Is my software an accessory? Telecommunication between HCP and patients EU Medical Device Regulations 10
K Verify Software Architecture - supporting interfaces between items IEC 62304 - Medical Device Software Life Cycle Processes 2
E ASTM F2118 - Fatigue testing of bone cement - Changes between the 2003 and the 2014? Other Medical Device Related Standards 1
A What is the difference between Design Process, Process Design and Design Control? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 2
R What's the major difference between Green Belt and Black Belt in term of training and project Six Sigma 3
DuncanGibbons How is the arrangement between Design and Production organisation envisaged? EASA and JAA Aviation Standards and Requirements 4
M Risk Analysis Flow - Confusion between ISO 14971 and IEC 62304 IEC 62304 - Medical Device Software Life Cycle Processes 8
T Difference between a subcontractor and a supplier ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 21
K %GRR was between 10-30% so we have to have a "backup plan" per auditor IATF 16949 - Automotive Quality Systems Standard 15
H Difference between Stainless Steel 316 ASTM F899 and ASTM A276 Other Medical Device Related Standards 3
A Exact terms for a plating failure and difference between rejection rate and failure rate Manufacturing and Related Processes 9
S ISO 13485 Lead Auditor - Debate between our Quality Team and Regulatory Auditor - Internal Auditor Training ISO 13485:2016 - Medical Device Quality Management Systems 17
M Difference between MSA and MSE? General Measurement Device and Calibration Topics 1
gramps What is the difference between discrete and continuous variables? Problem Solving, Root Cause Fault and Failure Analysis 3
R Plea for advice on transitioning between Notified Bodies (label updates) Medical Device and FDA Regulations and Standards News 1
M Measuring FIM (TIR) - Two inside diameters - Conflicting readings between inspectors Manufacturing and Related Processes 1
JoCam Difference between Approval and Registration - ISO 13485:2016 ISO 13485:2016 - Medical Device Quality Management Systems 2
S Difference between EU-MDR Annex IX and the Annex-combo X&XI EU Medical Device Regulations 4
T ISO 17025:2017 Clause 4.2.2 - The difference between "be notified" and "be informed" ISO 17025 related Discussions 4
Jimmy123 What is the difference between Error Proofing and Controls? ISO/IATF 16949 - Control Plans FMEA and Control Plans 16
DuncanGibbons Clear differences between ISO 13485 and AS 9100D requirements ISO 13485:2016 - Medical Device Quality Management Systems 10
H What is different between PED certificate and CPR certificate? Manufacturing and Related Processes 2
B Angle between two surfaces Inspection, Prints (Drawings), Testing, Sampling and Related Topics 0
D Variation between Faro Arms Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 2
K Differences between Manufacturing Process Audit & Layered Process Audit Lean in Manufacturing and Service Industries 4
P Risk acceptability alignment between ISO 14971 and IEC 62304 IEC 62304 - Medical Device Software Life Cycle Processes 6
C IEC 60601-1-8, difference between table 4 and annex D IEC 60601 - Medical Electrical Equipment Safety Standards Series 2
D Reorganizing responsibilities between management teams and Employees in them ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 7
A Compatibility between MDD and MDR devices EU Medical Device Regulations 7
Q How should I analyze measurement correlation between me and customer? Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 12

Similar threads

Top Bottom