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what is batch no. of prednisole tablet.
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Loss of linearity in tkn analysis, possible reasons?
In BP2013, Loperamid HCl monograph. Assay by titration with 0.1N sodium hydroxide using hydrocloric acid 0.01N and reading the volume added between the 2 points of inflexion. I have a question that if the diluent solvent is ethanol is certainly consumed a amount of volume of titrant, so this volume must be eliminated on the result calculation or not apart from first point which is subtracted above.
how to select short coloum and long coloumn for new molecule
UV and PDA detector, which have less signal to noise ratio?
how require to select dissolution media? what is discrimination?
how we can identify the impurity is coming below loq at transfering site?
What is the formula for relative diffrence for standard solution in solution stability in validation?
How can we calculate "confidence interval" in analytical method validation? Pl. explain with example.
process of Diclofenac sodium,IP.
My question about gas chromatography sulfur chemiluminsecence detector. I test unknown sample gas by GC-SCD (calibrated ) and the result of *H2S is 279 PPM , *but when I test the same sample with the GC-TCD (calibrated ) the value of *H2S is 2500 PPM . I'd like to inform you that both GCs are calibrated and have very good operation conditions with stable parameters . the question is if the sample gas with higher H2S over detection limits of SCD detector (1000 ppm). why the result it 279 ppm Best regards
in dissolution if one bowl got 70 percent 2nd bowl got 80 percent and 3rd bowl got 90 percent then how proceed?
Which parameter require to do for analytical method equivalency?
How can we confirm the HPLC column is end-capped or not? Is it possible to identify by physical appearance?
Why only 1.2 million lux hours require in photostability study?
AT WHAT CONDITIONS WILL YOU ANALYSE A SAMPLE,WHICH ARE PRESERVED AT OTHER THAN THE AMBIENT CONDITIONS?(ie COLD STORAGE SAMPLES BELOW 20* CENTIGRADE?
