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principle of dissolution
what is difference between temporary change control and deviation
What do you mean by Q+5 in dissolution?
how you can fix the known and unknown impurity limit for any drug substance
Which instrument used fbd fingerbag pore size identify purpose
What is the difference between Analytical method validation and Analytical method transfer?
How to select temperature of ODT in disintegration test
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?
Hai,i had completed my M.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 vislawath.jyothi@gmail.com
the international interview procedure for a job.
how impurity is analyzed in a tablet
what is the defination of Change Control given in various guidelines?
How we fix the validity period of a volumetric solution and re-standardization due date?
What is the difference between Deviation and Out of Specification?
What is pooled sample and why it is required in dissolution test?
