How quantitative stability studies are done?
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How melting point apparatus is calibrated?
What is the relative response factor in related substances?
Why we selecting 900 ml dissolution medium perticular drug as per I.P, USP?
2 Answers Akums, Torrent Pharma,
what is difference between temporary change control and deviation
what is limit of cleaning validation
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how related substnce method developted for new compound which not official in the pharmacopiea
what are all the needs or pre-requisites to perform project on bracketing and matrixing of stability products?
what do you mean by end capping
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In Stability testing if significant change occurs then what will be the action plan