Answer Posted / s.kumar
According to WHO,USP and ICH guidelines,inorganic metals present in the drugs should not be more than 10ppm.this inorganic metals are very dangerous to health.during ash test inorganic metals are converted to metal sulphates and are very stable at 600 degree celcious.below 600 degree celcious all the organic impurities will get evaporated.
Thanks,
B.Gangatharan
| Is This Answer Correct ? | 8 Yes | 0 No |
Post New Answer View All Answers
Why are use silicon oil mr?
before starting analytical method valodation what you checking? and how giving preference to start validation?
function of detecter in hplc ,gc and spectroscopy? function of carrier gas in gc?
in which situation require to change rs specification?
if identification threshold crosses the limits then what next step?
What is gelatinization?
How can we confirm the HPLC column is end-capped or not? Is it possible to identify by physical appearance?
What is the difference between chromatographic purity and related substances?
what is the principle of UV Vis spectroscopy, AAS, ICP OES,ICPAES, ICP-MS and FTIR
iam usig ph buffers merk. manually how to prepare ?
in which situation require to take incident in validation?
What is similarity factor?
What is a difference between potency and purity?
Why do we use KMnO4 in the test of control of obsorbance ? and why do we take specific quantity i.e 57-63mg?
what is diffrence between specificity and selecivity?