before starting analytical method valodation what you checking? and how giving preference to start validation?
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Why we are injecting low load standard conc. while analysing Related Substances by HPLC?
what is the difference between potentiometric assay and hplc assay
Data was integrated with RRT CONCEPT OR Overlay with SSTchrmatogram concept which is better?
we can use expired sample for validation and analyst qualification?
how can we determine RRF value in HPLC FOR CALCULATION OF IMPURITY ?
Why dissolution apparatus having 8 jars ?
What is the limit for single maximum impurity limit as per USP??
What is the diffrence between the performing of LOD ordinary drying at voven and vaccum method.
How is the Flame test performed?
what is the different in Total ash, sulphated ash, acid insoluble ash, alcoholic or non alcoholic ash?
In dissolution test s1 stage we are getting one bowl 40 % out of 6 bowls what is the root cause you find and how proceed next step? ( Q is 80%)
how to calculate the Step and ripple accuracy for pump gradient test for UPLC?