What is the process of migration to ISO 9001:2015?

B

bapatmn

#1
Hello All,

We currently hold ISO 9001:2008 QMS. Is the 9001:2008 standard is getting retired. If yes - what would be the next steps we would require to follow.

Do we need QMS upgrade to TICKIT or ISO 9001:2015.

Please suggest.

Regards,
Manoj
 
Elsmar Forum Sponsor

Ajit Basrur

Staff member
Admin
#2
Re: What is the process of migration to ISO 9001:2015 ?

Hello All,

We currently hold ISO 9001:2008 QMS. Is the 9001:2008 standard is getting retired. If yes - what would be the next steps we would require to follow.

Do we need QMS upgrade to TICKIT or ISO 9001:2015.

Please suggest.

Regards,
Manoj
Welcome to the Cove :bigwave:

You can go through multiple threads on ISO 9001:2015 Pre-Release Discussions here - http://elsmar.com/Forums/forumdisplay.php?f=221
 
#3
Re: What is the process of migration to ISO 9001:2015 ?

Hello All,

We currently hold ISO 9001:2008 QMS. Is the 9001:2008 standard is getting retired. If yes - what would be the next steps we would require to follow.

Do we need QMS upgrade to TICKIT or ISO 9001:2015.

Please suggest.

Regards,
Manoj
Yes, the 2008 is being "retired". The 2015 version of ISO 9001 will be available (if all goes to plan) 4Q 2015. Then you have 3 years to make the changes. I'm not sure that will happen to the TickIT scheme at the moment. But you WILL have to upgrade to ISO 9001:2015 by 2018.
 
B

bapatmn

#4
Re: What is the process of migration to ISO 9001:2015 ?

Thanks Andy and Ajit for your response.

We were under impression as our QMS 9001:2008 is little old now, it would reuqire upgrade by end of this financial year. But it seesm that's not the case.

Having said that, yes - as 9001:2015 is live we would need upgrade within 3 years span.

Regards,
Manoj
 

John Broomfield

Staff member
Super Moderator
#5
Re: What is the process of migration to ISO 9001:2015 ?

Manoj,

If your management system is already based on your organization's business processes then all you'll have to do is determine the additional processes and controls specified by the updated standards and determine:

1. The processes and controls you already have in place
2. The processes and controls you need to design and implement

Conversely, if your quality management system is written around the standards then now is the time to make it process-based.

Then you will be ready to quickly bring your organizational management system up to speed with changed system standards and newly adopted management system standards.

Even better, your colleagues will be running the business using their management system that naturally conforms to the standards.

John
 
#6
Re: What is the process of migration to ISO 9001:2015 ?

We were under impression as our QMS 9001:2008 is little old now, it would reuqire upgrade by end of this financial year. But it seesm that's not the case.

Manoj
Manoj - I'm a little concerned at this statement. You appear to suggest that you are only updating your system when the standard changes? Is this so?
 
A

aglowack

#7
Re: What is the process of migration to ISO 9001:2015 ?

Manoj,

It is a good idea to check with your registrar as well because they will stop issuing 2008 certificates before the 2018 date given by ISO. Most registrars won't have an answer for you until ISO 9001:2015 is officially released.
 
C

ChrisTGW

#8
Re: What is the process of migration to ISO 9001:2015 ?

I'd appreciate some feedback as well.....my company is beginning its ISO "Path" this year. We currently are NOT certified to any standard, so assuming 2015 goes "live" in January, 2016, would we have to certify to that Standard if we don't certify to 2008 by 31 December 2015?
 
Last edited by a moderator:
#9
Re: What is the process of migration to ISO 9001:2015 ?

No, Chris - you have until (March?) 2017 to implement and be certified to 2008
 
Thread starter Similar threads Forum Replies Date
N Sterilization Protocol Change in Validation Process and further impacts ISO 13485:2016 - Medical Device Quality Management Systems 1
N Riveting - special process Manufacturing and Related Processes 11
M Material incoming to the production process reflected in PFMEA FMEA and Control Plans 5
A API Spec Q1 Purchasing Process - Supplier Reevaluation based on Supplier Risks 5.6.1.4 Oil and Gas Industry Standards and Regulations 11
B Handling lower detection limits for SPC and process performance Statistical Analysis Tools, Techniques and SPC 1
S Approval Process for Disinfectant Sanitizers in Dubai Elsmar Xenforo Forum Software Instructions and Help 0
D Measurables for Plastic Injection molding process Manufacturing and Related Processes 1
S Cleaning process center change ISO 13485:2016 - Medical Device Quality Management Systems 4
Z Rapid audit template for plastic parts manufacturing process Manufacturing and Related Processes 12
R Inspection and Work order process Inspection, Prints (Drawings), Testing, Sampling and Related Topics 7
T ISO 13485:2016 Clauses related to process matrix ISO 13485:2016 - Medical Device Quality Management Systems 3
A How to reduce the process SPC monitoring Capability, Accuracy and Stability - Processes, Machines, etc. 3
John Predmore Configuration Management as a process instead of a procedure AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 6
R PCBA process validation Qualification and Validation (including 21 CFR Part 11) 2
U Internal Auditor not trained but done Audit for some process Nonconformance and Corrective Action 5
B Two excellent examples of process capability analysis from Quality Magazine Capability, Accuracy and Stability - Processes, Machines, etc. 5
D ECO (Engineering Change Order) process questions ISO 13485:2016 - Medical Device Quality Management Systems 7
S Sterilization validation after changing sterilization process provider Qualification and Validation (including 21 CFR Part 11) 3
Pau Calvo Quality Management process is mandatory in ISO9001? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 10
Tagin Template or Checklist for Process Change Document Control Systems, Procedures, Forms and Templates 5
LostLouie Manufacturer divorced from Design process, is he justified in design process deficiencies? ISO 13485:2016 - Medical Device Quality Management Systems 9
J 1.11 Preliminary Identification of Special Product and Process Characteristics APQP and PPAP 4
D Question regarding customer feedback process ISO 13485:2016 - Medical Device Quality Management Systems 3
T What does AS9100 mean when it says you must establish a process to do X? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 24
J Process FMEA Template with examples - Cold and Hot Forged components FMEA and Control Plans 4
D Questions regarding process validation ISO 13485:2016 - Medical Device Quality Management Systems 6
D Question regarding ECO process, specifically for Life Science products and defining form fit and function ISO 13485:2016 - Medical Device Quality Management Systems 1
P Managing How PPAP Requirements are Communicated in the Manufacturing Process and to Suppliers APQP and PPAP 5
I Control Plan (Product/Process specification/ Tolerance) acceptance FMEA and Control Plans 27
L Process changes and biocompatibility (ISO 10993-1) Other Medical Device Related Standards 1
A Validation of Forced Aeration Process ISO 13485:2016 - Medical Device Quality Management Systems 3
R Error Proofing Label process Manufacturing and Related Processes 4
B New Release of CQI-12 Coatings Process (Revision 3- Release date- 7/2020) Customer and Company Specific Requirements 2
D Layered Process Audits - FCA 9.2.2 - Exemption Clause? IATF 16949 - Automotive Quality Systems Standard 5
B ISO 11607-2 "Critical Parameter" vs. "Process Parameter" Other Medical Device Related Standards 6
Q Example Process orientation to the process leadership, management, goals (tasks of the top management) ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 10
S Process Inspection -Sub assembly process inspection sheet Lean in Manufacturing and Service Industries 3
T ISO 13485 8.3 - Non-Conforming Materials - on-line rework or part of process? ISO 13485:2016 - Medical Device Quality Management Systems 11
T Outsourced process in ISO 45001 Occupational Health & Safety Management Standards 3
L Manufacturing Process Audit Help IATF 16949 - Automotive Quality Systems Standard 6
T Formal Q Self Assessment - Problem with assigning Product and Process Customer and Company Specific Requirements 1
K Problems with process equipment ISO 13485:2016 - Medical Device Quality Management Systems 4
W Need for current design or process control FMEA and Control Plans 2
M Hiring Decisions - How much effort do you put into the hiring process these days? (7/2020) Misc. Quality Assurance and Business Systems Related Topics 6
hockeyhead Existing process never included in AS9100 scope of certification AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 10
A What is the difference between Design Process, Process Design and Design Control? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 2
V Process, component or full product re-qualification: leaded to unleaded solder Qualification and Validation (including 21 CFR Part 11) 8
C Refreshing an old and boring topic - Job descriptions and Roles vs Process Documentation ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 38
R Where does IATF 16949 address Process mapping? IATF 16949 - Automotive Quality Systems Standard 3
C OEE and In-process Inspection Manufacturing and Related Processes 2

Similar threads

Top Bottom