should cleaning be validated one single time and written in a protocol?
do we need to check the effectivness of the cleaning by analytical methods every time we clean the equipement?
do we have to write a cleaning validation protocol for each product?
Hi ankur, i’ve read your article on pharmaguideline on “cleaning method validation protocol”, i would like to ask for assistance on how will i conduct the placebo recovery… I’m not familiar with cleaning method validation…Before, i was conducting the assay method validation, and i know the specificity test wherein we add certain % amount of placebo on the product, and not the other way around where in we add the active on the placebo…I’m just a little bit confused on it…