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Answer Posted / karunasri
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If vendor having more imp than monograph then how to proceed? and how to set spec?
what is diffrence between specificity and selecivity?
how you confirm the assay method?
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?
how to develop the icp ms method? Application of icp ms?
what is mean by peak intigrity?
What is a difference between potency and purity?
why sre you used Potassium hydrogen phthalate in standarisation of 1N NaOH and 0.1 N Perchloric Acid?
what is mean by dissolution biowaiver study?
how to selecet an exact coloumn for an new molecule development by hplc how to select exact salt as buffer for new molecule development by hplc what is the the process to select the mode of saparation of compoundes by hplc what is the use of ph of buffer what is use of buffer,ph,organic phase,ans methods how the molecules get saparated in coloumn,
what is the principle involved in turbidometry and nephelometry ?
what is the importance of peak purity in HPLC and how we can calculate through manul(not software)?
in which situation require to use paddle and basket?
which are the sizes of capsules?
In which situation we require to analytical method validation of excipient?
