USP methodology, EP methodology, IP methodology, among three if possible to use one methodology for qualify working standard to use USP, EP, IP ? Please explain...
why sre you used Potassium hydrogen phthalate in standarisation of 1N NaOH and 0.1 N Perchloric Acid?
Related substance method equivalency on control sample or spiked sample?
In HPLC (Waters) software Empower1,2 &3 what is the updation for each version
in sampling of raw material which side is pasted sampled labels
Why only Copper standard is used to calibrate Atomic Absorption spectrophotometer?
Why dissolution test is not performed in all of the products
what is the structure of DOWEX-50
identification is for unknown? qualification for known? reporting for LOQ?
For titration in anhydrous media with perchloric acide, if lack of titrator, Which indicator is been used for replacement. How calculate pH of test solution to choose suitable indicator?
what is the acceptance criteria for enteric coated tablets in 0.1n hcl validation in each parameter?
Why we use potassium dichromate in uv calibration Exact reason behind it??
Why acetonitrile and water are used as extraction solvent when analysis melamine? I thought they are miscible and won't be able to separate...
in which situation require to take incident in validation?
Which is the highly polar and highly non polar column in HPLC?