SBS - The best value in QMS software

How many mandays needed for QS certificate renewal?

A

AllenLee

#1
#1
Hi friends,


Does any body can let me know how many manday needed for QS certificate renewal (our employee is 1500)
 
Standard Work Instruction Software by Dozuki
Elsmar Forum Sponsor
A

AllenLee

#2
#2
Re: Certificate renewal manday

Maybe this is a silly question, but i can not find it in QSR. Anybody can help me?
 
Marc

Marc

Hunkered Down for the Duration with a Mask on...
Staff member
Admin
#3
#3
Certificate Renewal Manday Requirements

Hang on - Have to check source for 'manday' requirements.

Others in the meantime?
 
Sidney Vianna

Sidney Vianna

Post Responsibly
Staff member
Admin
#4
#4
If I am not mistaken here, the IAF policy of 2/3 of the mandays for the Certification Audit should apply.

So, if it is for a design responsible organization with 1500 employees, the certification audit should have been 15 auditor-days, thus the re-certification audit should be at least 10 auditor-days on-site.
 
You must log in or register to reply here.
Thread starter Similar threads Forum Replies Date
S How many mandays required for the below mentioned standards IEC 27001 - Information Security Management Systems (ISMS) 3
S How many mandays are required for QMS audit? Internal Auditing 5
I How many mandays should the ISO9001 registration audit be? General Auditing Discussions 6
E Renewal of Certificate: How Many Mandays? Registrars and Notified Bodies 4
G Too many customer complaints Customer Complaints 14
I How many gauges in a Go/No Go Gauge? General Measurement Device and Calibration Topics 7
BeaBea How Many Processes should be created for each Department? Process Maps, Process Mapping and Turtle Diagrams 5
Watchcat How Many Notified Bodies are "Enough" Already? EU Medical Device Regulations 23
N MDR review process by notified body - How many steps exist in the review process EU Medical Device Regulations 0
F How many signatures do we need on calibration certificates? ISO 17025 related Discussions 8
M Informational From RAPS – Operating System Vulnerabilities in Many Medical Devices, Germany’s BfArM and Device Firms Warn Medical Device and FDA Regulations and Standards News 0
R Validation of Medical Device Hardware containing Software - How many to Validate ISO 13485:2016 - Medical Device Quality Management Systems 1
K How Many Samples to send for Chemistry Testing Pharmaceuticals (21 CFR Part 210, 21 CFR Part 211 and related Regulations) 3
N MDSAP Participants 2019 - How many companies are participating YTD? ISO 13485:2016 - Medical Device Quality Management Systems 20
S How many of you are using Robotic process automation for calibration lab management? ISO 17025 related Discussions 0
G Measuring customer parts on a CMM - How many decimals to report to the customer? ISO 17025 related Discussions 28
J Supplier choice limitation - Many of them dont have PSCR, VDA or even ISO 9001 VDA Standards - Germany's Automotive Standards 0
O Clean room performance qualification (pq) - How many times can I do each test? Manufacturing and Related Processes 8
G How many samples you require to test during PQ for validation of a equipment? ISO 13485:2016 - Medical Device Quality Management Systems 1
D IATF 16949: Do we have too many processes? Are they all the same? Registrars and Notified Bodies 7
D QMS Performance Based on how many NCRs were generated month to month Nonconformance and Corrective Action 8
S How many QMS processes and procedures? ISO 13485:2016 - Medical Device Quality Management Systems 2
L How many of you are Certified to IATF 16949 IATF 16949 - Automotive Quality Systems Standard 12
G How many Uncertainty Measurements for Micrometers and Calipers? Measurement Uncertainty (MU) 3
R How many Corrective Action Request can be Issued by DCMA for a single issue? Nonconformance and Corrective Action 2
A Training Program Help - Old docs, new docs, so many docs... ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 6
M How many Pieces to Test - Sterility Testing USP EU Medical Device Regulations 2
P Are we an outlier for so many variations of Change Management? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 4
M SPC with many data points from one dimension Statistical Analysis Tools, Techniques and SPC 16
S How many times do you have the term 'Requirements' in your Quality Manual? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 8
L How many working hours to required to implement ISO 14001 ? ISO 14001:2015 Specific Discussions 6
B ISO/TS16949 Internal Auditing - How many auditors? Internal Auditing 4
R Training Production Employees When We Have SOOO Many SOPs Training - Internal, External, Online and Distance Learning 9
P Scope Extension Audit - How many days? Do I audit all AS9100 requirements? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 2
J How can I manage Occurence Rates in FMEA efficiently when I have many processes? FMEA and Control Plans 9
V How many times the quality agreement has been invoked? ISO 13485:2016 - Medical Device Quality Management Systems 3
C How to document many document control systems with one Document Control Procedure? Document Control Systems, Procedures, Forms and Templates 6
A How many laboratories are accredited to ISO 17025 in the USA? ISO 17025 related Discussions 5
R Is it possible to randomly select samples from 1 column to many column Using Minitab Software 2
L How many ISO Standards are there and time allowed for Closing NCs? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 2
Ajit Basrur FDA - "We Moved Forward on Many Fronts This Year" - Margaret A. Hamburg, M.D. US Food and Drug Administration (FDA) 1
F AS9100 - How many times can the same auditor audit your system AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 1
J APQP Project Management in Excel - Many projects APQP and PPAP 8
S How many production runs will it take for SPC monitoring to stop? Statistical Analysis Tools, Techniques and SPC 10
M How many documents total do you currently have? Document Control Systems, Procedures, Forms and Templates 6
N How to Fix this Problem that is caused by so many different issues... Quality Tools, Improvement and Analysis 20
Ajit Basrur GHTF Releases many documents on Nov 5, 2012 ASQ, ANAB, UKAS, IAF, IRCA, Exemplar Global and Related Organizations 8
T How many complaints, defects and non-conformances are typical? Customer Complaints 5
A How many processes for an FDA Quality System (QSR)? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 7
B How many days after an interview should I follow up on the status of the interview? Career and Occupation Discussions 10

Similar threads

Top Bottom