Answer / suresh kumar

A Report raised during Quality System Audit on the
processes whenever it violates from the Quality System
Standards,Policies,Procedurs and whenever it fails to
deliver consistency in the Customer Satisfaction and
Continual Improvement.

Answer / jimdeli

A report outlining a deviation from product, process,
procedure, or compliance specifications.
Examples:

-A measured part dimension is spec'd to be .250" +/- .002.
It fails as measured at .257". It is a non-conforming part
and must be reported.

-An operator fails to follow procedure.

-A regulatory report is not filed on time.


The non-conformance report includes who, what, where, when.

The report generally initiates an investigation into Root
Cause (why).

It generally escalates to CAPA (Corrective and Preventative
Action) - steps to immediately correct and systemically
prevent (how) the non-conformance.

Answer / praveen

A failure to comply with a requirement of a company's
quality system standard.

Answer / rafael

it is a report outlning a deviation from
products,process,procedure or compliance specifications

Answer / pattan arshe ali khan

Failure to fulfill the requirement or procedure or other
relevent document has not been met then you have a non
conformance

Answer / rafael l dela cruz

Non-conformance reports shall be raised ations and
engineering standard requirements are violated in
material,workmanship or procedure.

Answer / balwan

Not complying th statutory requirement. or in other words
whatever the prequisite isignored by executor.

Answer / santhosh sebastian

Nonconformance:- Any product or material which does not
conform to the customer requirements or specifications,that
time we can raise Nonconformance against that
product/material.

Nonconformity:- When a process which does not conform to a
quality system requirement,That time we can raise
Nonconformity against that process(May be ISO stds,CMMi etc)

The Report we are sending to respective managers about
NC,is called NCR.This report contains NC and CAPA
(Corrective Action and Preventive actions)details along
with NC tracking and closing.Before sending NCR we should
check whether the correct process or specification
mentioned in Manual/PSD(Product Specification Documents)

Answer / adeeba

any unexpected:Action,occurrence,happening or situation
that has the possibility of affecting the
quality,potency,purity,safety or identity of the product.

Answer / sarnsh sahu

A report issued when a product, process or procedure does not comply with the set standards for a particular belonging to the product, process or procedure under inspection

What is basis set?

0 Answers  

at any application or software where the data will be stored at server side or at client side kindly answer it in detail?

1 Answers  

why do not u try to get job in your core side(example :-eee)?

0 Answers   Cap Gemini,

wat is compile module

1 Answers   QA,

How would you describe the involvement you have had with the bug-fix cycle between Development and QA?

1 Answers  

Why is it often hard for management to get serious about quality assurance?

0 Answers  

what is the diff between smoke testing & monkey testing?

9 Answers   Logica CMG,

Formal Testing?

2 Answers  

What if the application has functionality that was not in the requirements?

0 Answers  

'configuration related errors' in testing means what?

0 Answers  

what is mutation testing ? when we are using this type of testing?

0 Answers  

What is diffrence between iterative model and waterfall model?Explain What is the diffrence between iterative model and prototype model?Explain

6 Answers   IBM,