all types of questions asked at the cipla interview
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Which parameters require to do in tech transfer?
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When i inject amines and acid on HPLC then which peak will elut first?
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Whya the need of Specificity to do in Analytical Method Validation ?
What if impurity area in control sample coming more as compared to LOQ level of impurity ?
In chromatograpbic purity 90% is there, in assay 70% is there. How will you prove remaining 30%.
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