What is cleaning validation of rinse and swabe and its
limit with caculation formula.
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Sharmi+me = child
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UV and PDA detector, which have less signal to noise ratio?
How do we get end points and how many end points are possible for citric acid and di-acid not theorotically answer should be given practically.
before starting analytical method valodation what you checking? and how giving preference to start validation?
Why are use silicon oil mr?
what is the origin to prepare standard operating procedure
if peak get problamatic then what require to do?
how to set sample and standard concentration in RS method?
Basic principle of ESI?
which are the diffrent batches in the pharmaceuticals?
HI,I CLEARED BOB CLERK EXAM. MY INTERVIEW WILL BE ON 9TH OCTOBER,2010.PLEASE SEND ME INTERVIEW QUESTIONS AND ANSWERS. THANK YOU.
How doing qbd practically?
What is gelatinization?
what is procedure of actual procedure for registration of drug?
In rs method development when we are going area normalization method to dilute standard method?
Why we check moisture,ash & AIA in product