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 Categories >> Sciences >> Health Pharma >> Pharmacy
 
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Question Asked @ Answers Views     Select
What is the difference between Deviation and Out of Specification? cipla   0  722
In KF Standardization why we use Disodium Tartarate?    1  1836
What do you mean by CAPA?    1  2239
How quantitative stability studies are done? reddy-labs   0  1062
How we fix the validity period of a volumetric solution and re-standardization due date?    0  1211
What is the formula for KF standardization?    1  1613
Why should we not dispatch the reprocess material to export?    0  455
What are the limits for LOD and LOQ?    0  314
What are closely monitor parameters in stability study? reddy-labs   0  961
Why we use disodium tartare for determination of factor in karl ficher titration?    1  2522
What is pooled sample and why it is required in dissolution test?    0  264
What is photo stability?    2  1972
Why we use toluene for resolution in UV calibration?    1  7192
What is the difference between temporary change control and deviation?    0  345
Why 3X sampling plan are implemented in process validation?    2  2950
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Un-Answered Questions
 
 Question Views   Select
 
what is difference between uniformity of content and content uniformity as official test for tablet 849
why u want to join as a m.r? 835
when we calibrate uv for control of wavelength we scan for 200 to 800 nm but we get the result only for some specific wavelength how we confirm for all other wavelength? 525
why you choose pharmacy as a career what is pharmacists ideal job what is your goal in ur profession and how you achieve it 544
What is the relative response factor in related substances? 225
What is limit of cleaning validation? 258
What is the difference between Analytical method validation and Analytical method transfer? 336
Why and When RRF is necessary in RS method? How it is helpful in method development? 51
what are the limit of LOD and LOQ 2718
how to select HPLC column for a particular product 501
1.why did you choose this career 2.what is pharmacists ideal job 1004
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. 92
What is the difference between Calibration & Validation? 245
What do you mean by Bracketing and Matrixing in stability? 724
What is the difference between Blend uniformtiy and content uniformtiy ? 725
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