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Answer Posted / vasundhara,vijaya clg
michail tswett in 1906
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how require to fix the linearity and accuracy cincentration range?
Tell me about analytical method validation in QC
why salisylic acid not using now days for disdolution calibration?
If change in specification which parameter require to do for validation? if change in chromtographic condition then which parameter? if api change then which parameter? if change composition then which parameter? if old method not work out then whicj parameter? if additional one impurity added then which parameter of validation require to do on above each conditions? elaborate separately
why does used dry caffien in HPLC calibration?
what is the disso medium for tropsiun chloride
WHY given much noise PDA dector then VWD Dector
what is the purge flow & how to calculate
How to calculation of residual solvent methanol (3000 ppm) standard solution, and how many quantity used of test sample
How can we calculate "confidence interval" in analytical method validation? Pl. explain with example.
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
why xterra column require to use at higher ph?
what is the importance of peak purity in HPLC and how we can calculate through manul(not software)?
What are usp limits for theoritical plats,resoution,tailing factor,peak to valley ratio
