If we are getting split peak in Chromatogram,what we can do?
Answer Posted / n.s.r
In Method development time or already validated method first we conform that already validated method it's ok but in development time we go on peak purity and finalise column problem or if any impurities is present in main peak.Thank you ANY WAY YOU WILL answer that question.
| Is This Answer Correct ? | 0 Yes | 6 No |
Post New Answer View All Answers
What is the difference between purge septum flow and column flow in gas chromatography?
Why dissolution test is not performed in all of the products
How can the GC or HPLC method is selected to determine the impurity profile in drug product?
what are the guidelines for analytical method validations?
why should we perform dissolution PVT calibration only by UV spectrometer, not by HPLC ?
if identification threshold crosses the limits then what next step?
How would you decide dissolution medium for NCE compound of class I drug
what is mean by dissolution biowaiver study?
what is the procedure for cleaning of lenses of hatr accesory of ftir instrument?
which are the sizes of capsules?
i want model written test paper for the post of analyst in IOCL(indian oil corporation ltd) any one pls help me
if your product is soluble in 0.1n hcl and water then which you choose as media from these 2 media?
if rsd failed then what require to do?
Why we used in n-butyl acetate water content terminology while in ethyl acetate we used moisture content terminology?
what is mean by ambient temperature?