Answer Posted / kamaleshwar
Assay means the purity of the compound calculated aganist
a certified standard .That is a quantitative determination.
| Is This Answer Correct ? | 9 Yes | 3 No |
Post New Answer View All Answers
what is mean by dissolution biowaiver study?
what is difference between UV - VISIBLE MODEL NO like 1600,1601,1700 etc ? plz explain me
What is gelatinization?
What are usp limits for theoritical plats,resoution,tailing factor,peak to valley ratio
How you develop a method in HPLC?
[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?
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?
what is the origin to prepare standard operating procedure
In the isomers,enantiomers give the only physical properties present such that no chemical properties present.
in DMF having extra impurities and in api COA also having extra imp than USP or BP product then how require to proceed?
identification is for unknown? qualification for known? reporting for LOQ?
can we use the same detector in HPLC as well GC and what could be the differences we can find in the final chromato graph in any aspects?
which are the sizes of capsules?
what are risk assement in the analytical qbd?
why xterra column require to use at higher ph?
