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...

Can we interpret accuracy from linearity in method validation?

Answer Posted / jignesh

yes

Is This Answer Correct ?    0 Yes 0 No



Post New Answer       View All Answers


Please Help Members By Posting Answers For Below Questions

if rsd failed then what require to do?

877


Which parameters require to do in tech transfer?

819


for inorganic molecules require to do RS, Assay and disso?

774


function of detecter in hplc ,gc and spectroscopy? function of carrier gas in gc?

2721


how we can identify the impurity is coming below loq at transfering site?

930


in monograph 7 imp are there but in vendor showing 5 imp do not req to include 2 imp for that what will be justification?

783


inhouse product is in capsule form in combination and RLD is in tablet form then can we proceed for multimedia CDP? in inhouse capsule product disso is paddle with sinker in release media is there then RLD product in tablet form then with same as paddle with sinker we can proceed n.a.?

771


For standardization of volumetric solutions, acceptance limit for concentration is considered as 10% of nominal concentration and %RSD as NMT 0.2% (for appropriate no. of replicates). But , if %RSD has not met, what should be further action?

1960


identification is for unknown? qualification for known? reporting for LOQ?

776


How can the GC or HPLC method is selected to determine the impurity profile in drug product?

7676


In Dissolution Test why limit is define Q+5% what is the role of +5%.

3155


Which type of column should i use to check the purity of high molecular weight protein using HPLC reverse phase column chromatography? Hi everyone. I wanna to check the purity of high molecular weight protein (collagen) with MW of ~130 kDa using a HPLC. I know C18

1964


what is mean by covalidation

830


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

2212


How can we confirm the HPLC column is end-capped or not? Is it possible to identify by physical appearance?

3261