What is chiral and why this performing in HPLC
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if your impurity coeluting with each other in that situation how require to set specification? is it acceptable?
Please give idea about method development for cleaning method and how maco level establish
in gas chromatography what is the difference between gas flow rate and average linear velocity ?
What is diffrence between extractable volume and deliverable volume? Answer pls
why xterra column require to use at higher ph?
why cone formation during dissolution?
why sre you used Potassium hydrogen phthalate in standarisation of 1N NaOH and 0.1 N Perchloric Acid?
if your product is soluble in 0.1n hcl and water then which you choose as media from these 2 media?
why holium oxide prepared in 10% HCLO4 SOLUTION
what is impurity profile. how to interpret this impurity profile to a drug product or drug substance.
If suppose 10 methods of dissolution given in pharmacopoeial for single content product then which method out of 10? or all 10 require to follow?
If we do accuracy at same concentration at which linearity planned,what is the need to do linearity separately?
which are the sizes of capsules?
in which situation ion pair require to use?
how you confirm the assay method?