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What is limit of cleaning validation?
Describe some major trends in pharmaceutical field?
why we study matrixing in stability system in stability study and on what basis we select time point.
How would you make a physician to prescribe your medicine rather than that of the competitor?
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Whhat is the justification for stability study in api missed stations through deviations and statistical analysis is required.
Discuss the potential side effects and risks associated with Alprazolam usage. How would you manage or mitigate these side effects in a patient?
Why we use potassium hydrogen pthalate for determination of calibration in Total organic carbon
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?
i had completed my degree with 72% but i dont have good score in gre and tofel and i got an admission into a college in usa is trheir will be any problem if i appear for visa regection because of gre and tofel and i am from science background i lost touch in those subjects.
HOW TO PERFORM SATURATION SOLUBILITY IN DISSOLUTION METHOD DEVELOPMENT?
What should be Step wise the sterlization procedure for Dry Powder injection facility (from Starting)?
how related substnce method developted for new compound which not official in the pharmacopiea
how to make Enrofloxacin 20% solution & whats remedy to avoid crystal formation in this batch after 15 -20days? Please anybody assist in it
how you can fix the known and unknown impurity limit for any drug substance