Why dissolution test apparatus calibration with salycilic acid tablets was stopped by FDA&USP from the year of 2009?
1 9208Post New Analytical Chemistry Questions
How will u perform degradation study in detectors other thann PDA in HPLC Methodology
Why a1% value is used for some product ? What is the criteria for selection a1% value ?
why we use a particular hplc column for a particular compound give reasons?please
in sampling of raw material which side is pasted sampled labels
what is the structure of DOWEX-50
How to set specification of assay, fisdolution and related substances?
What is the calibration of uv process and preparation
What is the difference between chromatographic purity and related substances?
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?
How can I develope method of dissolution by HPLC OR UV
What is the difference between Discriminating media and DPDM(Dissolution Profile with Different Media)
What is the formula for relative diffrence for standard solution in solution stability in validation?
pharma industries oriented
What are usp limits for theoritical plats,resoution,tailing factor,peak to valley ratio
how to decide for one product require water content or LOD?