What is calibration procedure of gredient HPLC pump
Answer Posted / drena
Mobile phase A is 5.6mg/l of propylparaben in methanol (port
A and B)
Mobile phase B is 100% methanol (port C and D)
Run the test for 20 min by using curve 11 method
sample is Methanol
Acceptance criteria:
A/B/C is between 9.5 % to 10.5
A/B/D is between 9.5 % to 10.5
Is This Answer Correct ? | 13 Yes | 5 No |
Post New Answer View All Answers
How we performed the force degradation for drug substance, is any specific guideline is available for each parameter(Acidic, basic, oxidation,heat)? what conditions you mentained for above parameters.
What is related substance by HPLC impurity limits as per USP?
is it nessesary to do solution stability for 7 days?
what is definition of validation? which components are followed give detail?
why sre you used Potassium hydrogen phthalate in standarisation of 1N NaOH and 0.1 N Perchloric Acid?
Is it nessesary all multimedia dissolution require descriminatory?
on saturation solubility study data how we can find out the bcs class of drug?
What is the principle of HPLC, GC, LCMS, GCMS,LC QQQ, GC QQQ, LC Q TOF and GC Q TOF. What are the applications and Specificity?
what is impurity profile. how to interpret this impurity profile to a drug product or drug substance.
How require to develop GC method? how to select diluent, GAS, column selection and other chromatographic conditions?
What is the acceptance criteria for moisture balance when calibrated with sodium sulfate
is it necessary to do HPLC calibration at wavelength 315nm if we are doing analysis at this wavelangth
how the compound separate in coulunm,explain
How to calculate coreletion coefficient
[3/28, 20:52] Manoj P Venkatpurwar: how many impurities require to inject in assay specificity that how we can find out? and in Rs also how?