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How do we fix the sample concentaryion in hplc method development. What is the basis?
Why are use silicon oil mr?
If vendor having more imp than monograph then how to proceed? and how to set spec?
why require to do water content for drug product?
In which situation we require to analytical method validation of excipient?
in api coa contains only process impurities and in product coa contains degradation impurities?
if your impurity coeluting with each other in that situation how require to set specification? is it acceptable?
[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?
why holium oxide prepared in 10% HCLO4 SOLUTION
we can use expired sample for validation and analyst qualification?
on the basis of bcs class how to proceed the solubility?
WHY given much noise PDA dector then VWD Dector
What is the Formula for coreletion coefficient in plhplc calibration
if your product is soluble in 0.1n hcl and water then which you choose as media from these 2 media?
Which parameters require to do in tech transfer?
