difference between calibration and validation
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Why we used in n-butyl acetate water content terminology while in ethyl acetate we used moisture content terminology?
How to start the dissolution development for unknown tab?
How can we calculate "confidence interval" in analytical method validation? Pl. explain with example.
which one is better separation in high pressure liquide chromatogram orlowpressure chromato gram in hplc
how will you do the prep for unstable componds?
What is stray light in uv what are units for stray light
How to calculation of residual solvent methanol (3000 ppm) standard solution, and how many quantity used of test sample
cefoperozone and sulbactam inj. hplc test method
[3/28, 20:52] Manoj P Venkatpurwar: how many impurities require to inject in assay specificity that how we can find out? and in Rs also how?
pharma industries oriented
if you given one product then which tests you will perform?
AT WHAT CONDITIONS WILL YOU ANALYSE A SAMPLE,WHICH ARE PRESERVED AT OTHER THAN THE AMBIENT CONDITIONS?(ie COLD STORAGE SAMPLES BELOW 20* CENTIGRADE?
Why dissolution test is not performed in all of the products
before starting analytical method valodation what you checking? and how giving preference to start validation?
in which situation require to change rs specification?
