In dissolution test why sample is withdrawn from top of the
paddle and not less than 1 cm away from wall?
What is limit of uniformity of content as per USP?
What is the difference between sonication and homozinization?
How we fix the validity period of a volumetric solution and
re-standardization due date?
What is validation, validation protocol and validation
What is the difference between Analytical method validation
and Analytical method transfer?
how the qualification of pharma can help in banking
what are the limit of LOD and LOQ
what is difference between uniformity of content and content
uniformity as official test for tablet
how quantitative stability is done
What are closely monitor parameters in stability study?
what is difference between temporary change control and
What are the steps for the sterilization procedure for Dry
Powder injection facility (from Starting)?
how quantitative stability studies are done?
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.