Answer Posted / sreekanth
NANO3
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If we have 5 strength which is not dose proportinate and excipients also diffrent in each strength then how we can proceed for Force degradation? and excipient are same but not dose propotinate the how FD?
In which situation we require to prepare the standard solution from sample in Related substance method?
how you establish the LOQ?
if tech transfer fails whay require to do?
What is the difference between spectro meter and spectro photo meter?
[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?
What is the diffrence in japan mkt requirement in analytical method validation over US?
why are measure gas flow " ml " in Gas chromatography
Which parameter require to do for analytical method equivalency?
what is the acceptance criteria for enteric coated tablets in 0.1n hcl validation in each parameter?
could negative ions be produced by bombardment process in mass spectrometry?
in api coa contains only process impurities and in product coa contains degradation impurities?
how you fix the limits of impurities?
What should be the level/ Percentage of Arsenic in Arsenic free zinc.
How you develop a method in HPLC?
