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Chemistry AllOther (190) If inhouse hplc related substance method is completly diffrent from Usp for finished proďuct with diffrent impurities then how require to prove method equivalecy?
771analytical method validation require to with respect to release specification or shelf life specification?
791in monograph 7 imp are there but in vendor showing 5 imp do not req to include 2 imp for that what will be justification?
720In which situation we require to prepare the standard solution from sample in Related substance method?
777Hi sir if any product monograph not given known impurities (may be 5 impurities) specifications then how we require to proceed for inhouse formulation?
705
Define a substituted hydrocarbon?
What is the nature of the bonding interaction between a metal and an olefin? : Polymer Chemistry
Define an isomer?
how to prepare for the exam of ongc please give some idea
why are measure gas flow " ml " in Gas chromatography
what is turbidimetric titration?Give 2 examples.
if identification threshold crosses the limits then what next step?
What is the monomer of polyethene?
inhouse product is in capsule form in combination and RLD is in tablet form then can we proceed for multimedia CDP? in inhouse capsule product disso is paddle with sinker in release media is there then RLD product in tablet form then with same as paddle with sinker we can proceed n.a.?
How to calculate coreletion coefficient
Why there is no bond with 100% ionic character...??
Why is acetic acid added?
Ratio of Water and Acetonitrile(diluent) is not recommended to use in cleaning method validation,why?
What is the min constitutes of haematite ore?
How we choose the mobile phase for method development.?