How we performed the force degradation for drug substance, is any specific guideline is available for each parameter(Acidic, basic, oxidation,heat)? what conditions you mentained for above parameters.

2310

why we are using benzene, anyline in acetic anhdride assay titration method?

2115

please explian me about area normalisation method,diluted standard method,impurity vs impurity and which one has to be selected in method development

1632

How do we fix the sample concentaryion in hplc method development?

1140

Why we check moisture,ash & AIA in product

1885

IS THERE ANY EQUIPMENT TO CHECK AND CALCULATE THE POLARITY OF A LIQUID?

2457

before starting analytical method valodation what you checking? and how giving preference to start validation?

807

How do we quantify crystaline and amarpous forms by using (NMR, XRD)spectroscopic techniques? Which any others instruments are useful for this quantification? explain

2389

From where require to take the RLD sample?

756

how you determine moist.of NaOH sol or NaOH flacks

2222

in OSD forms require to use gas chromatography?

834

If change in specification which parameter require to do for validation? if change in chromtographic condition then which parameter? if api change then which parameter? if change composition then which parameter? if old method not work out then whicj parameter? if additional one impurity added then which parameter of validation require to do on above each conditions? elaborate separately

856

why salisylic acid not using now days for disdolution calibration?

772

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?

3356

analytical method validation require to with respect to release specification or shelf life specification?

793