What is the formula for Tapdensity /
- 6 Answers
- 15282 Views
- Dr Reddys, GR Intrachem, I also Faced
- E-Mail Answers
Answer Posted / murari
Tapped Density- W/V
where W is weight of sample
V is final tapped volume
this is as per USP
| Is This Answer Correct ? | 10 Yes | 1 No |
Post New Answer View All Answers
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
How do we fix the sample concentaryion in hplc method development. What is the basis?
why should we perform dissolution PVT calibration only by UV spectrometer, not by HPLC ?
Which is the highly polar and highly non polar column in HPLC?
is it nessesary to do solution stability for 7 days?
what are the guidelines for analytical method validations?
how the compound separate in coulunm,explain
in which situation require to use paddle and basket?
why salisylic acid not using now days for disdolution calibration?
How can I develope method of dissolution by HPLC OR UV
if you have given a blank water how you analyse by general analytical techniques?
I have compare C2H2-air and C2H2-N2O flame AAS on determination calcium. Both use same range of std to plot calibration curve. (2-6ppm) When i measure the sample with phosphate, KCl and LaCl, C2H2-N2O flame give false positive result, around 0.5ppm. When i measure the sample with phosphste, KCl and EDTA. C2H2-N2O flame also give 0.5ppm false positive. But both above mentioned sample would not give false positive when measured by C2H2-air flame. What is the reason?
How they found 1mL of K.F reagent is equivalent to 5mg of water and if we change the composition of K.F reagent, is it can neutralize more amount of water?
how you fix the limits of impurities?
