Golgappa.net | Golgappa.org | BagIndia.net | BodyIndia.Com | CabIndia.net | CarsBikes.net | CarsBikes.org | CashIndia.net | ConsumerIndia.net | CookingIndia.net | DataIndia.net | DealIndia.net | EmailIndia.net | FirstTablet.com | FirstTourist.com | ForsaleIndia.net | IndiaBody.Com | IndiaCab.net | IndiaCash.net | IndiaModel.net | KidForum.net | OfficeIndia.net | PaysIndia.com | RestaurantIndia.net | RestaurantsIndia.net | SaleForum.net | SellForum.net | SoldIndia.com | StarIndia.net | TomatoCab.com | TomatoCabs.com | TownIndia.com
Interested to Buy Any Domain ? << Click Here >> for more details...

How precise should be the linearity in HPLC method validation?

Answer Posted / premraj behera

Based on the final concentration of the samples/standards
used for the validation of the method, homogeneity and
stability, the linearity plot (Concentration Vs Area) will
be plotted which covers the final concentration with ± 50%
range. so that analyzed concentration of the
samples/standards will fall within these range which is
acceptable.

Is This Answer Correct ?    2 Yes 0 No



Post New Answer       View All Answers


Please Help Members By Posting Answers For Below Questions

How to decide assay range for non pharmacopeial API analysis by HPLC? Could you give me any reference for same e.g Guidelines or Paper publications?

3395


acceptance criteria for lod & loq by standard deviation of response and slope??

2639


Colorimtry

1696


what is difference between UV - VISIBLE MODEL NO like 1600,1601,1700 etc ? plz explain me

2723


if peak get problamatic then what require to do?

858


Which are the diffrent grades of api in pharma?

813


please explain about aluminium hydroxide assay

1178


what is mean by peak intigrity?

1022


How do we quantify crystaline and amarpous forms by using (NMR, XRD)spectroscopic techniques? Which any others instruments are useful for this quantification? explain

2436


how to calculate elemental impurities?

1081


why cone formation during dissolution?

844


what is difference in ods I ods II is this is realy from sorbent / packing characteristics or from other means

2008


which one is better separation in high pressure liquide chromatogram orlowpressure chromato gram in hplc

2210


Qc interview questions

1789


we can use expired sample for validation and analyst qualification?

859