Why 1800 ml of dissolution media used In Carbamazepine ER USP Tablets But other drug only 900 ml Media Used ?
1 5487Post New Analytical Chemistry Questions
how you establish the LOQ?
Is it nessesary all multimedia dissolution require descriminatory?
about method developement in hplc
How to set analyticl specification for combination products?
In which situation we require to analytical method validation of excipient?
what is the origin to prepare standard operating procedure
what is third integration
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?
For standardization of volumetric solutions, acceptance limit for concentration is considered as 10% of nominal concentration and %RSD as NMT 0.2% (for appropriate no. of replicates). But , if %RSD has not met, what should be further action?
How to start the dissolution development for unknown tab?
What is the formula for relative diffrence for standard solution in solution stability in validation?
for inorganic molecules require to do RS, Assay and disso?
what is %labelled amount in content uniformity of dosage unit and its calculation?
what is classification of elemental impurities? what is risk assement in elemental impurities?
Why sometime potassium ortho phosphate mix with acetone use for sample preparation for hplc