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 Categories >> Sciences >> Health Pharma >> Pharmacy
 
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Question Asked @ Answers Views     Select
What do you mean by end capping? sun-pharma   1  3467
How will you calculate telling in any HPLC peak?    1  3297
What is capacity factor?    2  2173
If calibration of 12 bowl dissolution apparatus does not meets single stage procedure, how can you precede calibration?    0  1167
How related substance method is developed for new compound which is not official in the pharmacopeia?    0  1032
What is limit of uniformity of content as per USP?    0  909
What is the difference between uniformity of content and content uniformity as official test for all tablets?    0  431
What is the difference between sonication and homozinization?    0  465
What is the difference between polarimeter lamp and IR lamp?    0  2108
How melting point apparatus is calibrated?    1  1199
What is the difference between Analytical method validation and Analytical method transfer?    0  335
How polarimeter is calibrated?    0  262
What is the calibration of HPLC?    0  384
What is GMP, cGMP and GLP?    1  3997
What is the difference between mix-up and cross-contamination?    0  1880
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Un-Answered Questions
 
 Question Views   Select
 
In dissolution test why sample is withdrawn from top of the paddle and not less than 1 cm away from wall? 550
What is limit of uniformity of content as per USP? 909
What is the difference between sonication and homozinization? 465
How we fix the validity period of a volumetric solution and re-standardization due date? 1201
What is validation, validation protocol and validation master plan? 528
What is the difference between Analytical method validation and Analytical method transfer? 335
how the qualification of pharma can help in banking 113
what are the limit of LOD and LOQ 2702
what is difference between uniformity of content and content uniformity as official test for tablet 846
how quantitative stability is done 604
What are closely monitor parameters in stability study? 955
what is difference between temporary change control and deviation 360
What are the steps for the sterilization procedure for Dry Powder injection facility (from Starting)? 1410
how quantitative stability studies are done? 1621
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. 83
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