what are the guidelines for analytical method validations?
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what is a drug?
How precise should be the linearity in HPLC method validation?
why we are performing residue on ignition?
How did you conclude that when stressing a compond, all degradation products have eluted in chromatogram?
What is the meaning of Base deactivated vials
what are the important specifications for a Column ?
What is the purpose of performing dissolution test on routine basis?
When we r doing processing method for sst in Empower software by HPLC, What value has to give in void volume and as per which pharmacopia!
What is chiral and why this performing in HPLC
key components in hplc?
If i performing one analysis on C8column then the same analysis done on C18 column then what will happen about Rt;Resulution;Peak shape Explain ?
in DMF having extra impurities and in api COA also having extra imp than USP or BP product then how require to proceed?