Can we interpret accuracy from linearity in method validation?
What is similarity factor and its use in api strength?
U have 4 strengths have different coating meterial which one u chose to do forced degradation stady in validation
Why base line not start from zero in GC Chromatography analysis.
What is the column performance and column efficiency?
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.?
if the purity is 99.9%,is need to do assay?
which are the guidelines for force degradation studies?
According to ICH,India is coming under which climatic zones?
difference between precision & accuracy.
For limit test of heavy metals in BP, Method C require that the substance is ignited at a temperature not exceeding 800 °C. Why confines such the temperature?
WHAT IS THE DIFFERENT BETWEEN PURITY, POTENCY AND ASSAY
why the same column give different retention time in hplc?