If vendor having more imp than monograph then how to proceed? and how to set spec?
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In pharmacopeal solibility parameter of a material, is et essential to test all paramete? If 70-75% parameter passes can we assess that the material is satisfactory or not?
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give clarity of linearity and range in method validation
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why does used dry caffien in HPLC calibration?
if you have given one product then how you determine the impurity in that?
What is the reason of RT change in new column v/s old column in HPLC
what is the source of ir spectroscopy
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