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Answer Posted / kjjg
in unipune
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What if impurity area in control sample coming more as compared to LOQ level of impurity ?
how decide the clining method and cleaning method validation require for this perticular products?
Why six unit used for precision?
which are the diffrent batches in the pharmaceuticals?
what is the acceptance criteria for enteric coated tablets in 0.1n hcl validation in each parameter?
In HPLC (Waters) software Empower1,2 &3 what is the updation for each version
Did anybody have method for acetyl cysteine effervescnce tablet
Explain the relations between number of carbon atoms in alkanes and retention time ?
In IR spectra, generally a molecule vibrates without apply emr or ir light?
what is classification of elemental impurities? what is risk assement in elemental impurities?
on saturation solubility study data how we can find out the bcs class of drug?
in gas chromatography what is the difference between gas flow rate and average linear velocity ?
As per ICH related substances stability trend limit from initial to shelf life
If inhouse hplc related substance method is completly diffrent from Usp for finished proďuct with diffrent impurities then how require to prove method equivalecy?
we are performed SOR for a particular product the limit is -6 to -10.We face particular bathes it is not meeting the specification.we performed diffrent instrument diffrent analyst we are getting diffrent diffrent results.solvent is dimethyl sulfoxide what could be the reasion
