In pharmacopeal solibility parameter of a material, is et
essential to test all paramete? If 70-75% parameter passes
can we assess that the material is satisfactory or not?
if out of two set of results of moisture analysis first 1 is passing, second one is failing, is it oos ? or vice a versa first 1 is failing and second one is passing. for information mean value to be reported and in mean value the substance is ppassing, is it oos or normaal mean value to be considered?
how do you established the RRF for unknown impurity
What is difference between Chromatographic purity and Related substances analysis?
What is UV cut off?
How to calculate the signal to noise ratio.
which situation gc hs and gc als require to use?
what is mean by ambient temperature?
What is NPOC method in TOC?
What is pooled sample in Dissolution
2 Answers Graviti Pharmaceuticals, Lupin,
WHY given much noise PDA dector then VWD Dector
in loss on drying Why follows on constant weight not more than 0.5 mg, any region
What are the different zones in stability according to ICH?