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...

At what distance the sample is collected in dissolution
basket?

Answer Posted / praveen vyas

As per usp sample should be drawn from middle of the basket or paddle upper surface and dissolution medium level and 1 cm away from jar wall

Is This Answer Correct ?    1 Yes 0 No



Post New Answer       View All Answers


Please Help Members By Posting Answers For Below Questions

analytical method validation require to with respect to release specification or shelf life specification?

733


what is the different in Total ash, sulphated ash, acid insoluble ash, alcoholic or non alcoholic ash?

9926


in dissolution why pool sample needed? in which type of drug pool sample need?

3135


is it nessesary to do solution stability for 7 days?

718


mahagenco syllabus for the post of chemist

6426


WHY pKa value is more important than pH value of the mobile phase in HPLC?

1712


AT WHAT CONDITIONS WILL YOU ANALYSE A SAMPLE,WHICH ARE PRESERVED AT OTHER THAN THE AMBIENT CONDITIONS?(ie COLD STORAGE SAMPLES BELOW 20* CENTIGRADE?

2013


Which products will produce when acetic anhydride reacts with Ter-butanol, Sec-butanol, Iso butanol, Dimethylamine etc.

2829


In which situation we require to analytical method validation of excipient?

732


What are the primary considerations in extractables and Leachables ?

2214


[3/28, 20:52] Manoj P Venkatpurwar: how many impurities require to inject in assay specificity that how we can find out? and in Rs also how?

745


What are usp limits for theoritical plats,resoution,tailing factor,peak to valley ratio

1850


pharma industries oriented

2172


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

808


If we have 5 strength which is not dose proportinate and excipients also diffrent in each strength then how we can proceed for Force degradation? and excipient are same but not dose propotinate the how FD?

757