Why 1800 ml of dissolution media used In Carbamazepine ER USP Tablets But other drug only 900 ml Media Used ?
1 5560Post New Analytical Chemistry Questions
While performing TOC sst analysis Zero shift disabled & sample analysis zero shift enabled why?
What is dose dumping? why require to do?
How to decide assay range for non pharmacopeial API analysis by HPLC? Could you give me any reference for same e.g Guidelines or Paper publications?
why xterra column require to use at higher ph?
how to decide for one product require water content or LOD?
How to set specification of assay, fisdolution and related substances?
what is lod and loq ?,why use k2cr2o7 , kcl h2so4 in uv calibration ?,why use benzophenone & caffene acetone in hplc calibration ?,what is leading peak in hplc ?why we do the calibration of limit of stry light in hplc & uv ?
Why are use silicon oil mr?
How much is the standard area for glc analysis
why require the ph, buffer during hplc mobile phase?
if your impurity coeluting with each other in that situation how require to set specification? is it acceptable?
For standardization of volumetric solutions, acceptance limit for concentration is considered as 10% of nominal concentration and %RSD as NMT 0.2% (for appropriate no. of replicates). But , if %RSD has not met, what should be further action?
Tell me something about Vitamin A test method by HPLC
in DMF having extra impurities and in api COA also having extra imp than USP or BP product then how require to proceed?
How to calculate coreletion coefficient