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how we do assay of urea, ammonium sulpate, ammonium nitro
pospate etc
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What is dose dumping? why require to do?
why glutent are detected in the rice cereal baby food product even manufacturer claimed that they are using rice and milk only?we have using ELISA to do the test,and rice supposed not containing any glutent,rite?We already repeat the test so many times and it still detected.just wondering where the glutent came from?
in which situation ion pair agent require to use?
why octanol used to determine the partition coefficient ?
What is the formula to determine the concentration of M of a solution given the % transmittance? Use %T = 43.7 as an example.
In HPLC Calibration, On which basis RSD Limit of noise test is fixed (NMT 33.0 % )
what is impurity profile. how to interpret this impurity profile to a drug product or drug substance.
How can we calculate "confidence interval" in analytical method validation? Pl. explain with example.
what is definition of validation? which components are followed give detail?
how require to fix the linearity and accuracy cincentration range?
how you start the solubility study?
what parameters we will consider while developing a HPLC method and how we confirm our HPLC method is valid?
what is mean by ambient temperature?
how you confirm the assay method?
in DMF having extra impurities and in api COA also having extra imp than USP or BP product then how require to proceed?
