if your impurity coeluting with each other in that situation how require to set specification? is it acceptable?
923Post New Analytical Chemistry Questions
which batch require to use for analytical method validation?
what are risk assement in the analytical qbd?
sop of a uv visible spectrophotometer double beam elico model
from where i get mortar pastle for glass bottle crush? it's required for testing of it?
if tech transfer fails whay require to do?
what is impurity profile. how to interpret this impurity profile to a drug product or drug substance.
all types of questions asked at the cipla interview
in which situation ion pair agent require to use?
What is dose dumping? why require to do?
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?
why we use a particular hplc column for a particular compound give reasons?please
effect of pore size, pore volume, partical size, column length, carbon load on retention time? what is carbon load? what is the use?
how many types of balance calibration test?
Which are the diffrent grades of api in pharma?
analytical method validation require to with respect to release specification or shelf life specification?