What is the limit for single maximum impurity limit as per USP??
Hi sir if any product monograph not given known impurities (may be 5 impurities) specifications then how we require to proceed for inhouse formulation?
What is Specificity ?
what is the difference between c-8 and c-18 column
How will decide to use HPLC OR GC for developing method for unkown compund
how you establish the LOQ?
What is viod volume and peak purity in HPLC?
what is mean by dissolution hydrodynamics?
why we use only sucrose in the calibration of polarimeter?
In performance Check of GC Why Hexadecane Peak is Considered
0 Answers Asian Paints, MSN Pharma,
Column selection in HPLC method development?
In GC Why does retention time decrease when temperature increases? Also how does a change in temperature effect selectivity?
Why we are using K2Cr2O7 for control of absorbance in UV?