Answer Posted / hari
Quantitatively determination of amount of main component of a sample present in substance.
| Is This Answer Correct ? | 15 Yes | 2 No |
Post New Answer View All Answers
how will you do the prep for unstable componds?
How to calculate coreletion coefficient
how you fix the limits of impurities?
before starting analytical method valodation what you checking? and how giving preference to start validation?
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?
what is classification of elemental impurities? what is risk assement in elemental impurities?
What is the diffrence in japan mkt requirement in analytical method validation over US?
What if impurity area in control sample coming more as compared to LOQ level of impurity ?
How to calibration of the uv spectroscopy and its test?
In HPLC Calibration, On which basis RSD Limit of noise test is fixed (NMT 33.0 % )
What is the acceptance criteria for moisture balance when calibrated with sodium sulfate
Why dissolution test is not performed in all of the products
how many types of balance calibration test?
How require to develop GC method? how to select diluent, GAS, column selection and other chromatographic conditions?
If inhouse hplc related substance method is completly diffrent from Usp for finished proďuct with diffrent impurities then how require to prove method equivalecy?
