What if impurity area in control sample coming more as compared to LOQ level of impurity ?
No Answer is Posted For this Question
Be the First to Post Answer
some compound havving uv region but not give much more response during hplc analysis
If we have 5 strength which is not dose proportinate and excipients also diffrent in each strength then how we can proceed for Force degradation? and excipient are same but not dose propotinate the how FD?
why should we perform dissolution PVT calibration only by UV spectrometer, not by HPLC ?
is it necessary to do HPLC calibration at wavelength 315nm if we are doing analysis at this wavelangth
How can we determine Moisture content of HI?
What is the name of the detector used in TOC?
what is %labelled amount in content uniformity of dosage unit and its calculation?
Why linearity of detector performed in HPLC calibration
give clarity of linearity and range in method validation
what is the results if we use ODScolumn instead of BDS column ,(ther parameter is same for column) in assay method ?
What is gelatinization?
How do we fix the sample concentaryion in hplc method development?