Answer Posted / swati
We can qualify unknown impurity in RS method by spiking standard component in placebo...preparing sample solutions for accuracy and linearity depending upon specification limit of unknown impurity.
| Is This Answer Correct ? | 0 Yes | 2 No |
Post New Answer View All Answers
What is diffrence between extractable volume and deliverable volume? Answer pls
how to select short coloum and long coloumn for new molecule
what is mean by ambient temperature?
what is turbidimetric titration?Give 2 examples.
Why a1% value is used for some product ? What is the criteria for selection a1% value ?
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?
For titration in anhydrous media with perchloric acide, if lack of titrator, Which indicator is been used for replacement. How calculate pH of test solution to choose suitable indicator?
i want model written test paper for the post of analyst in IOCL(indian oil corporation ltd) any one pls help me
What are usp limits for theoritical plats,resoution,tailing factor,peak to valley ratio
why we are using benzene, anyline in acetic anhdride assay titration method?
In HPLC Calibration, On which basis RSD Limit of noise test is fixed (NMT 33.0 % )
Home heating oil or furnace oil what is made from? Can (base oil plus diesel/kerosen) = home heating oil?
we can use expired sample for validation and analyst qualification?
In performance Check of GC Why Hexadecane Peak is ConsideredÂ
for inorganic molecules require to do RS, Assay and disso?