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This video is prepared to make all of you understand key expectations from different guidelines. For that purpose, 3 questions are identified every week and answered in line with current guidelines.
In this video, the questions answered are;
1. Is it required to evaluate the variability in residue levels during cleaning validation?
2. During cleaning validation, Do we have to wait for swab and rinse samples to be approved prior to using the equipment for production?
3. During MACO (Maximum Allowable Carry Over) calculation, Do we have to use a safety factor depending on the nature of the formulation?
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