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How we can identify process related and degradation impurity in single method with short period?
How to set specification of assay, fisdolution and related substances?
USP methodology, EP methodology, IP methodology, among three if possible to use one methodology for qualify working standard to use USP, EP, IP ? Please explain...
in which situation require to change rs specification?
in which situation require to take incident in validation?
if peak get problamatic then what require to do?
how you confirm the assay method?
From where require to take the RLD sample?
Tell me about analytical method validation in QC
Which are the diffrent grades of api in pharma?
if instrument calibration fails then what require to do?
how you determine moist.of NaOH sol or NaOH flacks
In Assy by potentio metry titration method how select MET U ,DET U, SET U,
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If vendor having more imp than monograph then how to proceed? and how to set spec?
