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what is the difference between Tailing Factor & Asymmetry
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How would you decide dissolution medium for NCE compound of class I drug
what is mean by peak intigrity?
Many times I don't got a caffeine peak in calibration of hplc using guard column ❓
How require to perform linearity as per ANVISA? What are the acceptance criteria?
How to set analytical specification for combination products?
what is impurity profile. how to interpret this impurity profile to a drug product or drug substance.
Is it nessesary all multimedia dissolution require descriminatory?
in dissolution why pool sample needed? in which type of drug pool sample need?
What is intact assay method development.....?
What is column in chromatography?
How to do regeneration of Metacarb Pb plus column?
in which situation ion pair require to use?
Did anybody have method for acetyl cysteine effervescnce tablet
How to establish relative response factor for hplc. Why it is required?
If inhouse hplc related substance method is completly diffrent from Usp for finished proďuct with diffrent impurities then how require to prove method equivalecy?
