If granules are over lubricated what defect arises in tablet compression how we solve this problem.819
why dissolution multimedia profile of drug is important. what are the specifications for tablets ,capsules,powders etc1633
why we study matrixing in stability system in stability study and on what basis we select time point.1050
How to select temperature of ODT in disintegration test
What is column efficiency and performance ? And how can we know the column is better?439
principle of dissolution1497
what is the exact classification of pharmaceutical industry (area wise) as per cleaning limits(Class A.B.C.D)539
Why disintegration of uncoated tablets is 15 minutes why not 16 or 14 or any other value .1 1743
What is the Disintegration time for Hard gelatin Capsule in USP?
What should be Step wise the sterlization procedure for Dry Powder injection facility (from Starting)?
HOW TO PERFORM SATURATION SOLUBILITY IN DISSOLUTION METHOD DEVELOPMENT?
what is purpose of slow,medium,fast sampling in process validation ?
When we change water of Hygrometer?
What is the difference between uniformity of content and content uniformity as official test for all tablets?
How many types of impurites in Related compound test?
plz if anyone have a model question papers for exam of drug inspector than plz send me on my E-mail ID email@example.com
In Stability testing if significant change occurs then what will be the action plan?
Why we use pyrene in HPLC calibration ( UV-vis/PDA)
what are all the parameters to be considered while applying bracketing and matrixing?where and all it is applicable?
What is the difference between Deviation and Out of Specification?
What is pooled sample and why it is required in dissolution test?
why we are using toluene in resolution in UV calibration
Why we are using propyl parabben in methanol in calibration of hplc for GPV test??