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...

In standard weight box used for calibration of analytical
balance there are two numbers (Qty) of 20mg, 200mg,2.oGM
weights. Why?

Answer Posted / nilesh

in box u receive 1,2,5,10,20,50,100,200,500
now for 30 mg u able to use 10+20. but what about 40mg,90mg,140mg,190mg,400mg

Is This Answer Correct ?    8 Yes 2 No



Post New Answer       View All Answers


Please Help Members By Posting Answers For Below Questions

If we do accuracy at same concentration at which linearity planned,what is the need to do linearity separately?

2313


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

2399


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.?

721


What is viod volume and peak purity in HPLC?

2889


How they found 1mL of K.F reagent is equivalent to 5mg of water and if we change the composition of K.F reagent, is it can neutralize more amount of water?

1784


What is similarity factor and its use in api strength?

1308


Colorimtry

1672


How require to perform linearity as per ANVISA? What are the acceptance criteria?

1349


what is mean by ambient temperature?

932


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

804


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

4287


how require to interprit the method precision data of hptlc?

831


what is the principle of UV Vis spectroscopy, AAS, ICP OES,ICPAES, ICP-MS and FTIR

9259


how you fix the limits of impurities?

846


in stress study if your api not soluble in hcl naoh h2o2 then what require to do?

847