in api coa contains only process impurities and in product coa contains degradation impurities?
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How we performed the force degradation for drug substance, is any specific guideline is available for each parameter(Acidic, basic, oxidation,heat)? what conditions you mentained for above parameters.
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why we use polystyrene film for ftir calibration?
Identify problem faced when mass spectroscopy is used with HPLC system ?
0 Answers College School Exams Tests,
what type of questions asked on analytical balance and also give answers................all pharma companies?
What is the difference between Optical rotation and Spcefic optical rotation
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How we develop a method by HPLC for unknown compound,if we got three peaks with same response then how we can find out which one is our desired compound's peak without taking help of LC MS.
what is mean by UOD?
which effect is mainly responsible for chromatographic separation when silica is the statinary phase at TLC? thanks in advance
what is mean by Q in S1 and S2
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