Transition-Support.com's Website - TS 16949 Information

Elsmar Forum Sponsor
P

pdboilermaker

#3
Bwoods:
There are also companies on this great forum that are registered to this technical spec. If you have specific questions perhaps someone from thes companies could help

General Seating of America
ISO/TS 16949
ISO 14001
Registered company
 
B

BWoods

#4
Originally posted by pdboilermaker:
Bwoods:
There are also companies on this great forum that are registered to this technical spec. If you have specific questions perhaps someone from thes companies could help
Registered company
Thanks for the offer.

Just always on the lookout to learn more. So do searches from time to time on the internet. Came across that site and wanted to share it with you good people. I already know what a great forum this is. That is why I made sure to post that URL for you all.

Talk with you later.

Bill
 
I

isodog

#5
Why on earth would anyone want to convert a QS-9000 system to ISO 16949? It's is more work, doesn't appear to be value added, And has considerable added costs. I'm not trying to be cute, I just don't understand.
Is this demand coming from customers?

Dave
 

Marc

Hunkered Down for the Duration
Staff member
Admin
#6
Originally posted by isodog:
Why on earth would anyone want to convert a QS-9000 system to ISO 16949?
Because pretty soon there will be no QS-9000.
 
I

isodog

#7
Then WAIT! Money spent tomprrow costs you less than money spent today. I see NO added value!

Dave
 

Marc

Hunkered Down for the Duration
Staff member
Admin
#9
Originally posted by isodog:
Then WAIT! Money spent tomprrow costs you less than money spent today. I see NO added value!
Unfortunately, like a disease, waiting often costs much, much more. A planned, incremental transition shouldn't cost you any significant money. If a company needs a consultant for the transition it's only because they don't have the appropriate expertise in-house. Any company which doesn't have the in-house expertise deserves to pay a consultant - they're on the cheap anyway.

Take a brief read through Elsmar.com/ubb/Forum1/HTML/000307.html When folks write things like "...Yes Richard did work with our group and he was a God send, we couldn't have gotten registered without his guidance. He helped set up a system, and generate an attitude in the organization that truly bought into the benefits of a fully implemented Quality Management System. You consultants provide such a valuable service that is all too often unrecognized as being necessary by the management teams of most companies I've had experience with...." By the way, Rich was one of the folks I brought into Motorola's Phoenix registration project.

A good consultant can save a company significantly - in time and money, both in the short term and in the long term. Companies might not like paying us, but they do have the option of hiring personnel full time who are qualified to do the work they pay us to do.

Remember, we're not making the rules. We don't require you to do ISO or whatever. A company chooses to do so and it is their option whether to accomplish their goal with internal personnel or with consultants.

You say: "...Then WAIT!..." By all means. wait until the last minute. Nothing like reactionary, last minute firefighting as opposed to an orderly, timely transition. That's always the cheapest way, right?

You say: "... I see NO added value!..." If you plan to be supplying the automotive industry 3 to 5 years from now you will not have a choice whether it's 'value added' or not. For many companies right now QS and ISO are not value added - except in so far as sales goes. No QS - no sales to GM, Ford or Chrysler. Harley didn't do the ISO dance because they wanted to or because it is to them value added - Germany and several other european countries threatened to stop imports. Harley had no choice - it was related to sales, not any additional value to their company. They may say otherwise - but I know the facts. I was there.
 
Thread starter Similar threads Forum Replies Date
T Brexit Transition Arrangements & Import into the EU EU Medical Device Regulations 3
J MDD to MDR transition - Time required for the implementation of the MDR EU Medical Device Regulations 7
S MDR consultants - in search of recommendations for a consultant for MDR transition. Paid Consulting, Training and Services 7
K Annex XVI Device Transition Timeline under the MDR EU Medical Device Regulations 2
B ISO 9001:2015 Transition: Much Easier Than You Think! Misc. Quality Assurance and Business Systems Related Topics 0
M UDI transition period and implementation EU Medical Device Regulations 6
M Informational The US FDA is Recommending Transition to Duodenoscopes with Innovative Designs to Enhance Safety: FDA Safety Communication Medical Device and FDA Regulations and Standards News 0
O New MDR 2017/745 Transition Strategy - 2019 Manufacturing and Related Processes 3
A How to manage the QMS system and SOP during the transition from MDD to MDR EU Medical Device Regulations 4
S When is the last date for transition to ISO/IEC 80079-34:2018? Other ISO and International Standards and European Regulations 0
K CE mark transition and new regulations CE Marking (Conformité Européene) / CB Scheme 0
Ronen E Informational ISO 13485:2016 Transition Period End - 1 March 2019 ISO 13485:2016 - Medical Device Quality Management Systems 0
T MDR Guidance Book - Useful for MDR transition? EU Medical Device Regulations 1
M Medical Device News EU – Transition Timelines from the Directives to the Regulations – Medical Devices and in vitro Diagnostic Medical Devices Medical Device and FDA Regulations and Standards News 13
H Transition to ISO 13485:2016 together with ISO 9001:2015 ISO 13485:2016 - Medical Device Quality Management Systems 12
Ed Panek Transition to IEC 60601 4th Edition - Risk Analysis and test submissions CE Marking (Conformité Européene) / CB Scheme 2
M Medical Device News Health Canada - Medical Device Single Audit Program (MDSAP) Transition Plan Canada Medical Device Regulations 2
M Medical Device News FDA News - 26-09-18 - FDA Reveals Vision for the Transition to ISO 13485 Other US Medical Device Regulations 1
M MDSAP Transition - Health Canada Website Notice on Apr 13 2018 Canada Medical Device Regulations 1
O IEC 60601-1-2 4th edition transition deadline Dec 31 2018 CE Marking (Conformité Européene) / CB Scheme 1
qualprod Transition and recertification at the same time? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 3
P How To Transition From AS9100c to AS9100 Rev. D AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 6
A ISO 14001:2015 transition from the 2004 standard ISO 14001:2015 Specific Discussions 8
F IATF 16949:2016 transition audit - Internal Audit Closures IATF 16949 - Automotive Quality Systems Standard 13
W AS9120A to AS9120B transition AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 5
L Transition date to IEC 60601-1-11:2015 IEC 60601 - Medical Electrical Equipment Safety Standards Series 1
Q Surveillance Audit of 2008 before Transition Audit to ISO 9001:2015 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 20
B Going into IATF 16949 transition without Internal Audits IATF 16949 - Automotive Quality Systems Standard 4
pammesue We have done NOTHING toward the ISO 9001 transition ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 19
S Management representative transition checklist IEC 27001 - Information Security Management Systems (ISMS) 7
O ISO 9001:2015 Transition Internal Audit completion thread ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 16
A ISO 14001:2015 transition audit - Major NC due to the procedure and audit plan ISO 14001:2015 Specific Discussions 10
T ISO 9001:2008 to 2015 transition - How much work to change? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 14
R ISO 9001:2015 Transition Quality Manual Update - Redundant Content ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 12
G Upkeep of ISO 9001:2008 during Transition TO ISO 9001:2015 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 5
D AS9110 Re-Certification & Transition Audit AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 0
S Is there enough time left to transition to ISO 13485:2016 and MDSAP? ISO 13485:2016 - Medical Device Quality Management Systems 1
M AS9100 Rev. D Transition Audit - Number of Audit Days AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 5
G Effect of ISO9001 2015 transition on ISO IEC 80079-34 Other ISO and International Standards and European Regulations 2
R Who here is Using a Consultant for ISO 9001 Transition? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 2
Sidney Vianna One year to ISO 9001 and 14001 transition deadline. ISO & IAF communique' ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 12
Sidney Vianna IATF bringing stakeholders together to ensure Transition by the 2018-09-14 deadline IATF 16949 - Automotive Quality Systems Standard 10
D Number of Audit Days - AS9100D Transition for a Small Shop AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 3
Ronen E Transition to MDR (EU 2017/745) - I'd like to make an offer EU Medical Device Regulations 12
Q Presentation for Employees - Starting the ISO 9001:2015 Transition ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 2
K AS9100 Rev. D Transition - Internal Audits & Gap Analysis Requirements AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 14
M Who has had a Transition Audit from TS 16949 to IATF 16949 IATF 16949 - Automotive Quality Systems Standard 120
S Question for those who have completed Transition Audit for ISO 9001 ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 7
O Guidance and/or assistance on Transition to AS9100 Rev D AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 11
M Multi-Site Umbrella Certification Transition Plan ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 1

Similar threads

Top Bottom