Interested to Buy Any Domain ? << Click Here >> for more details...
Answer Posted / vaishali musale
The specificity of the method was determined by analyzing
standard drug &test samples.the purity of the drug
determined by comparing Three regions i.e. peak start peak
apex & peak end.
| Is This Answer Correct ? | 4 Yes | 3 No |
Post New Answer View All Answers
How to set analytical specification for combination products?
what is the purge flow & how to calculate
if you given one product then which tests you will perform?
what is definition of validation? which components are followed give detail?
what is mean by dissolution hydrodynamics?
We use hicrome 10 cxs column in hplc analysis....pls tell me.. what is the meaning of 10 cxs?
why does used dry caffien in HPLC calibration?
What is shaking level in GC?
how you start the solubility study?
what parameters we will consider while developing a HPLC method and how we confirm our HPLC method is valid?
why multimedia dissolution require to do?
What is rs test why we are performing rs test?
why lactose has less charges when packed in steel containers when compared with packing of lactose in polyamide material?
Why we select scan range from higer wavelength to lower wavelength in uv visible spectroscopy and ftir spectroscopy ? .
how you establish the LOQ?
