if your impurity coeluting with each other in that situation how require to set specification? is it acceptable?
What is delay volume?
Why only hydroxy naphthol blue indicator is used for standardisation of 0.05M EDTA solution instead of solochrome Black T or Euriochrome Black T indicator which is used for all sample analysis with 0.05M EDTA solution?
What is column in chromatography?
in which situation require to change rs specification?
Why sodium hydroxide used for maintain pH of phosphate buffer
can i use hplc detector to uplc and why?
why glutent are detected in the rice cereal baby food product even manufacturer claimed that they are using rice and milk only?we have using ELISA to do the test,and rice supposed not containing any glutent,rite?We already repeat the test so many times and it still detected.just wondering where the glutent came from?
what are risk assement in the analytical qbd?
What is the principle of Thermal conductivity detector and FID?
what is the structure of DOWEX-50
Identify problem faced when mass spectroscopy is used with HPLC system ?
please explian me about area normalisation method,diluted standard method,impurity vs impurity and which one has to be selected in method development
how to set sample and standard concentration in RS method?
Did anybody have method for acetyl cysteine effervescnce tablet