Transition from QS to TS with Different Registrars

A

AirAusquin

#1
#1
Transition from QS to ISOTS:2002 with different registrars

Hi to all, this is my first post here, I have a question:

I am working with a QS Certified manufacturer in Venezuela, South America, which corporate offices are in the US. We are transitioning to ISO/TS 16949:2002 as a corporate decision.

Some background info:
- Our QS Registrar, a US company, has communicated us that they have quit from working outside the US territories.
- We have contacted a new registrar for ISO/TS
- Our last (annual) surveillance audit was on last November.
- Our QS certificate shows that it is valid until July 2004.
- We have been toll that we will be deslisted with our current registrar on November 2003.
- Our schedule for ISO/TS places our certification audit early on December 2003 (no way to make it sooner)
- We have been told by the new registrar that now recommendation letter is issue when registering to ISO/TS and that the certificate will take 2-3 months to be issued.

My questions are:
What will happen with our certification status while we wait for the new certificate?
Which are our options?

Thanks in advance for any help

Alejandro Irausquín
 
Standard Work Instruction Software by Dozuki
Elsmar Forum Sponsor
howste

howste

Thaumaturge
Super Moderator
#2
#2
AirAusquin said:
My questions are:
What will happen with our certification status while we wait for the new certificate?
Which are our options?
Click to expand...
The short answer is that you will not be certified from November until you get the new certificate. If being certified is a requirement for you to do business with your customers, that could be a major issue for your company.

It seems like your options are:
1) let your certification expire & deal with the consequences
2) have your new registrar do a QS-9000 surveillance audit before your certificate is delisted and have them issue a new QS-9000 certificate
3) find a way to get your TS certification audit done earlier

BTW, why can't they audit you before November?
 
S

Sam

#3
#3
AirAusquin states,
"- Our QS certificate shows that it is valid until July 2004.
- We have been toll that we will be deslisted with our current registrar on November 2003."

Your new registrar can pick up the balance of your QS with a desk audit and a modest fee. They may require a pre-assessment audit.

"- Our schedule for ISO/TS places our certification audit early on December 2003 (no way to make it sooner)"

Once your new registrar picks up your QS this will be plenty of time.

"- We have been told by the new registrar that now recommendation letter is issue when registering to ISO/TS and that the certificate will take 2-3 months to be issued."

I can't speak for all registrars, but ours completed the process and we had our certificate within thirty days.
 
A

AirAusquin

#4
#4
Thanks guys! :)

We discussed this further and came to the conclusion than the safer way to go is doing the QS assesment with the new registrar. It will cost us more but we will stay in the safer side.

Alejandro
 
You must log in or register to reply here.
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