when will be the drug inspector notification will be
anounced.what are the educational requirements...
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Why we use 10 tablets for the analysis of cu test?
Describe some major trends in pharmaceutical field?
Disintegration time for soluble tablet
when will andhara pradesh government announces drug inspector posts and when will be the exam conducted? please inform me..
Why we use toluene for resolution in UV calibration?
how will convience the doctor
What is validation, validation protocol and validation master plan?
What is the difference between Validation & Qualification?
how impurity is analyzed in a tablet
How would you make a physician to prescribe your medicine rather than that of the competitor?
what is limit of cleaning validation
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.