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.
1 3957what type of lubricant oil should be apply on idle machine& storage of dies punch? What type of oil used on punch barrel?
1 10274Why and when RRF is required to be known in RS Method? How is it helpful during method development?
3 6914Why we use potassium hydrogen pthalate for determination of calibration in Total organic carbon
2138How to measure each & every tablets hardness in compaction force control system of compression machine?
2171what are all the parameters to be considered while applying bracketing and matrixing?where and all it is applicable?
2120what are all the needs or pre-requisites to perform project on bracketing and matrixing of stability products?
2052
what are the most common infectious diseases a pharmacist sees? Do pharmacists routinly encounter antibiotic resistent in some of the infectious agents that patients have contacted? if so which onces?
what is the defination of Change Control given in various guidelines?
Imagine a patient expresses a strong preference for Alprazolam due to its rapid onset of action. How would you address their request while considering their overall well-being?
define the starting material?
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Why we said Glacial Acetic Acid to Acetic Acid m
hai,i had completed my b.pharmacy.i want the coaching centres for drug inspector exam at hyderabad,pls help me nd wen wil b the DI exam conducted in 2012 mostly,pls also forward the model papers.. pls reply me at pravaliden@gmail.com
what are all the needs or pre-requisites to perform project on bracketing and matrixing of stability products?
what is difference between uniformity of content and content uniformity as official test for tablet
What is difference between assay and content uniformity ?
Discuss the potential side effects and risks associated with Alprazolam usage. How would you manage or mitigate these side effects in a patient?
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What is the difference between temporary change control and deviation?
what is difference between temporary change control and deviation
if one drug is acidic in nature and the other drug is basic in nature, e.g. desloratadine is soluble in acidic environment i.e 0.1N HCL whereas Montelukast Sodium is soluble in basic environment i.e. .2% SLS. How can we choose a common media for there Dissolution?