why cone formation during dissolution?
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What attracted you to analytical chemistry?
If inhouse hplc related substance method is completly diffrent from Usp for finished proďuct with diffrent impurities then how require to prove method equivalecy?
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...
0 Answers Srini Pharmaceuticals,
why base line not starts from zero in gc?
1 Answers Aurobindo, FDC, Reddy Labs,
my name is santhosh i cmpleted b.pharmacy in 2009 then i went to uk in 2010 to pg diploma business management. after i came back to india.. recently again apply to uk for pharmaceutical analysis. they refused my visa you failed to explain y u r change subject. so plz ineed answer for y change the cource
What is basic difference between method validation,process validation
When you get Moisture content by KF higher than by LOD, what does this indicate?
why we are doing seal wash and needle wash?
Why we use methanol as solvent in kf standardisation. Why not other solvent?
2 Answers Caplin Point, Epione Labs, Hetero,
from where i get mortar pastle for glass bottle crush? it's required for testing of it?
IF WE INCREASE FLOW RATE RT DECRESE.WHY
What is the difference between specified impurity and Identified impurity