Defining context of the organization in IATF 16949
Our is carbon black producing plant, going for IATF 16949 . How can I write on context of organisation?
Modification of the Quality Manual in IATF 16949
I want to know about the modifications needed, Quality Manual modification from TS 16949 to IATF 16949.
Mandatory documents and risks and opportunities in processes
I would like to know which are mandatory procedures required to IATF 16949. Also would like to know how to identify risk and opportunity in the processes.
Retention of tooling records
What is the meaning of "control of records shall satisfy................production part approvals ,tooling records..............shall be retained for the length of time that the product is active for production and service requirements plus one calendar year....
Mandatory records and retention time in IATF 16949
Just curious is you would have an example of a list of mandatory documents required by IATF and their retention periods?
Making the transition to IATF 16949
I am looking for some guidance as I am preparing our plant for IATF 16949:2016. We have certificate TS 16949:2009. We are a stamping company.
Quality manual in IATF 16949
Some idea of how I will proceed for Quality Manual preparation for Quality Manual of this new standard (IATF 16949 :2016) what are the essential requirement
Changes in Quality Policy per IATF 16949
We have our Quality Policy as per TS 16949:2009. We are heading for IATF standard. What are the changes I have to do in our Quality Policy?
Process validation in IATF 16949:2016
Requirement of validation of processes for production and service provision in IATF 16949. Earlier clause 7.5.2 was in ISO/TS 16949
Risks with IATF 16949 implementation
How & What risk to be consider while implementation IATF 16949 ,as we are certified for ISO/TS16949?