How we performed the force degradation for drug substance,
is any specific guideline is available for each
parameter(Acidic, basic, oxidation,heat)? what conditions
you mentained for above parameters.
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differnc btw c18 and c-8 column
If we have 5 strength which is not dose proportinate and excipients also diffrent in each strength then how we can proceed for Force degradation? and excipient are same but not dose propotinate the how FD?
What is the pilot-plant in pharma sector.
U have 4 strengths have different coating meterial which one u chose to do forced degradation stady in validation
Which column is more polar, C8 or C18?
6 Answers Cipla, Glenmark, Laurus, Torrent Power,
what is mean by profiling of dissolution
In chromatograpbic purity 90% is there, in assay 70% is there. How will you prove remaining 30%.
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why plane of polarized light rotated by opticaly active compunds?
what are the normalisation, internal standard and external standerd methods in HPLC.
what is impurity profile. how to interpret this impurity profile to a drug product or drug substance.
what is difference between GC & GC-HS
Organic Chemistry 
