Why forced degradation studies are performed in hplc method
validation?

Answer Posted / sridhara h s

Evaluate stability of sample solution by repeatability in
one day (short time) or over days (long time).
Solution of sample must be stable for purpose of routine
analysis under normal laboratory conditions. Stability of
sample is important when a sample is under different
storage conditions.
Stability of sample needs special attention for gradient
analysis, requiring even 100 min or so. Mobile phase should
be selected to avoid stability problem.

Is This Answer Correct ?    5 Yes 24 No



Post New Answer       View All Answers


Please Help Members By Posting Answers For Below Questions

in DMF having extra impurities and in api COA also having extra imp than USP or BP product then how require to proceed?

348


What is third generation HPLC Columns?

1507


how pda detector works over uv?

286


how require to interprit the method precision data of hptlc?

295


in OSD forms require to use gas chromatography?

331






sop of a uv visible spectrophotometer double beam elico model

5349


which batch require to use for analytical method validation?

331


Loss of linearity in tkn analysis, possible reasons?

802


Why we select scan range from higer wavelength to lower wavelength in uv visible spectroscopy and ftir spectroscopy ? .

457


what is classification of elemental impurities? what is risk assement in elemental impurities?

340


Related substance method equivalency on control sample or spiked sample?

304


CAN WE DETERMINE THE PEAK PURITY IN GAS CHROMATOGRAPHY ANALYSIS?

704


in monograph 7 imp are there but in vendor showing 5 imp do not req to include 2 imp for that what will be justification?

265


What is the principle of Thermal conductivity detector and FID?

2259


What is the accrptance criteria in RSD for RS method precision on basis of impurity percentages?

307