What do you mean to CAPA?
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Answer / dillip palai
Corrective action and preventive action (CAPA, also called
corrective action / preventive action) are improvements to
an organization's processes taken to eliminate causes of
non-conformities or other undesirable situations[1]. CAPA is
a concept within good manufacturing practice (GMP). It
focuses on the systematic investigation of the root causes
of non-conformities in an attempt to prevent their
recurrence (for corrective action) or to prevent occurrence
(for preventive action).
Corrective actions are implemented in response to customer
complaints, undesired levels of internal nonconformity, non
conformities identified during an internal audit or adverse
or unstable trends in product and process monitoring such as
would be identified by SPC. Preventive actions are
implemented in response to the identification of potential
sources of non-conformity.
To ensure that corrective and preventive actions are
effective, the systematic investigation of the root causes
of failure is pivotal. CAPA is part of the overall quality
management system (QMS).
| Is This Answer Correct ? | 14 Yes | 0 No |
Answer / ali
corrective action and Preventive action (CAPA)
this is a question from SQA. this could be in the Audit
Process. there could be a CAPA log for every NC.
| Is This Answer Correct ? | 6 Yes | 0 No |
Answer / nilanjan saha
Corrective action and Preventive action is abbreviated as
CAPA.Its is a process to maintain the production process in
better manner.Corrective actions and preventive measures are
taken to hinder the earlier errors not to get into the system.
Internal audits takes place to verify we are following the
standards or not,and to analyse what actions should be taken
to improve the Standard.
As a whole it is a part of Quality management System(QMS).
| Is This Answer Correct ? | 2 Yes | 2 No |
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