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what is meant by CAPA?what is the source for deviation
(unplanned) to occur, though the process developed by
standard validation procedures?
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- GSK GlaxoSmithKline, I also Faced
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Answer Posted / deepika singh, ipqa, navdeep b
Corrective action and preventive action. No process
deviation shall be permitted under standard validation
procedures, but if occur likedeviation in the grade of
active raw material could affect the process parameters and
other critical quality attributes of formulation.
additional testing and revalidation should justify such
deviations
| Is This Answer Correct ? | 2 Yes | 0 No |
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