Dear all,
I know this topic must be kept in forum for many times, but still I need
your suggestions. If our compressed air is not coming directly in to product
contact (It may come indirect in processing such as filter integrity), up to
what level, the system needs to be validated? Is it sufficient to validate
the system with microbial monitoring or all chemical, dew point, oil free,
Microbial, particulate free challenge tests needs to be verified? Any
guideline available from WHO, EU, US???
Thank you very much,
Nimesh Solanki
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