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...

Whya the need of Specificity to do in Analytical Method
Validation ?

Answer Posted / rc

The specificity of an analytical method is basically to

1) To prove the stability indicating ability of the method

2)To identify the possible degradation of the molecule

3)To determine the type of degradation the molecule is
susceptible to

4)To prove the mass balance

5)To know the various degradation path ways of molecule

Is This Answer Correct ?    11 Yes 2 No



Post New Answer       View All Answers


Please Help Members By Posting Answers For Below Questions

Please tell me about the pH of Polycaboxylic ether is it in the 5-6 range ever or more than 6

2609


what is %labelled amount in content uniformity of dosage unit and its calculation?

5236


why we use a particular hplc column for a particular compound give reasons?please

2752


WHICH STANDARD WE USE IN SILICA ANALYSIS IN SILICA-GEL METHOD FOR SOLID SAMPLE

2132


Difference between hlaf and rlaf

2110


when we talk about change in entropy we consider total entropy means of surround +entropy of system but when we talk about change in Gibss free energy we consider entropy of system.explain with reason.

2042


How can we calculate "confidence interval" in analytical method validation? Pl. explain with example.

4268


How to do regeneration of Metacarb Pb plus column?

2580


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

2669


If change in specification which parameter require to do for validation? if change in chromtographic condition then which parameter? if api change then which parameter? if change composition then which parameter? if old method not work out then whicj parameter? if additional one impurity added then which parameter of validation require to do on above each conditions? elaborate separately

856


if you have given one product then how you determine the impurity in that?

744


how you establish the LOQ?

795


what is mean by nitrosamine impurities?

1069


USP methodology, EP methodology, IP methodology, among three if possible to use one methodology for qualify working standard to use USP, EP, IP ? Please explain...

2015


What is similarity factor and its use in api strength?

1299