Cleaning In Place

How can I do cleaning in place (CIP) validation for pharmaceutical ?
Is there someone who has a reference or help for this topic

CIP is basically first executed by the supplier and further inhouse modification and factors are involved in it.
CIP involve number of programmed cycle/stages in order to provide a cleaned equipment.
All the cleaning process parameters are set and defined by supplier and verified by production/QA validation as per the production requirements and worst case product.
Once everything is finalised, you can proceed for Cleaning validation accordingly (3 runs).


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