What is limit of cleaning validation?
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What do you mean by Q+5 in dissolution?
What is the storage condition for reference standard?
why we are using toluene in resolution in UV calibration
How to select HPLC column for particular product.
what is the exact diff betwen the uniformity of weight & uniformity of content?
How to conduct Literature Survey for Generics Development for European Market
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If an enteric coated tablet is taken with milk,will it disintegrate in stomach or still it will manage to pass into the intestine and disintegrate in inherent alkaline environment of intestine?
If we get 100% assay of an Initial sample ,and the stability studies of the same sample got 90% dissolution result, and when the same stability sample was analyzed for RS studies no impurities was found . Where the 10% Active substance were gone during dissolution analysis.Please help me in getting the conclusion.
What is the difference between sonication and homozinization?
WHEN WILL GUJRAT GOVERNMENT ANNOUNCES DRUG INSPECTOR POSTS AND WHEN WILL BE THE EXAM CONDUCTED? INFORM ME AND ALSO EAMINATION DATE