Validation of cleaning procedures has generated considerable discussion since agency documents, including the Inspection Guide for Bulk Pharmaceutical ...
Know what is cleaning validation, maximum allowable carryover ( MACO), acceptance criteria and recovery factor in cleaning validation.
Know about the procedure for cleaning validation and cleaning validation protocol and reports as per WHO. Method of sampling, Analytical methods and limits of ...
Cleaning validation is just as important as process validation when it comes to the safety and continued compliance of any manufacturing firm.
A lifecycle approach can be used to develop GMP-compliant cleaning procedures for continuous manufacturing of solid-dosage pharmaceuticals.