How you will select the runtime in HPLC for a drug in
method development.
- 6 Answers
- 19946 Views
- Aurobindo, GVK, Lesanto Laboratories, I also Faced
- E-Mail Answers
Answer Posted / ajay vishwakarma
depends on the last possible impurities in compound; which
should be confirmed at the time of method development.and
degradation Study,further Run time 5.0times more W.r.t to
Analyte Peak
| Is This Answer Correct ? | 4 Yes | 2 No |
Post New Answer View All Answers
what is difference between UV - VISIBLE MODEL NO like 1600,1601,1700 etc ? plz explain me
How to calculation of residual solvent methanol (3000 ppm) standard solution, and how many quantity used of test sample
what is biorelivent dissolution media?
Why sodium hydroxide used for maintain pH of phosphate buffer
In which situation we require to analytical method validation of excipient?
which one is better separation in high pressure liquide chromatogram orlowpressure chromato gram in hplc
what is mean by nitrosamine impurities?
why sre you used Potassium hydrogen phthalate in standarisation of 1N NaOH and 0.1 N Perchloric Acid?
acceptance criteria for lod & loq by standard deviation of response and slope??
what is diffrence between specificity and selecivity?
for which product require to do content uniformity? what is limit of cu?
how require to interprit the method precision data of hptlc?
in sampling of raw material which side is pasted sampled labels
Basic principle of ESI?
How we can identify process related and degradation impurity in single method with short period?
