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which are the sizes of capsules?
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how you start RS method development when for new product?
Why forced Digradition Study is done
In rs method development when we are going area normalization method to dilute standard method?
stability study is going on up to 3years for famotidine-USP but the pharmacopeia is revised and tlc test is replaced with hplc test. At the 4th year frequency the product is failed in hplc test .how can i assain the expiry or retest date and can i stop or continue the programme?
how many types of balance calibration test?
Why we are use 0.005M Sulphuric acid, in control of absorbance performance test UV Spectrophotometer calibration
why we should take dst factor for below 1%moisture samples
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if v use HELIUM & ARGON instead of NITROGEN as a mobile phase what happen in GC SYSTEM ?
What is the difference between low pressure gredient and high pressure gredient in hplc instrument?
how you fix the limits of impurities?
what is pK & pKa value
Why dissolution apparatus having 8 jars ?
Organic Chemistry 
