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IN DISSOLUTION WE ARE USING A LETTER 'Q' WHAT IS MENT BY Q
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if tech transfer fails whay require to do?
how to decide for one product require water content or LOD?
What is the difference between chromatographic purity and related substances?
function of detecter in hplc ,gc and spectroscopy? function of carrier gas in gc?
which batch require to use for analytical method validation?
what are the guidelines for analytical method validations?
In which situation we require to prepare the standard solution from sample in Related substance method?
How do we get end points and how many end points are possible for citric acid and di-acid not theorotically answer should be given practically.
In which situation we require to analytical method validation of excipient?
why should we perform dissolution PVT calibration only by UV spectrometer, not by HPLC ?
What is dose dumping? why require to do?
Identify problem faced when mass spectroscopy is used with HPLC system ?
in api coa contains only process impurities and in product coa contains degradation impurities?
in sampling of raw material which side is pasted sampled labels
what is the principle involved in turbidometry and nephelometry ?
