Answer Posted / ramalingeswararao
OOS is two types
1. Valid OOS
2. Invalid OOS
OOT Also two types
OOT is happend due to human error
OOT is happend due to product behaviour
Is This Answer Correct ? | 2 Yes | 0 No |
Post New Answer View All Answers
how to develop the icp ms method? Application of icp ms?
What is related substance by HPLC impurity limits as per USP?
How doing qbd practically?
in which situation ion pair require to use?
What is the accrptance criteria in RSD for RS method precision on basis of impurity percentages?
what is difference in ods I ods II is this is realy from sorbent / packing characteristics or from other means
why salisylic acid not using now days for disdolution calibration?
why xterra column require to use at higher ph?
Why use only methanol,used determinationof moisture content not use other solvents
As per ICH related substances stability trend limit from initial to shelf life
1.What is the difference between method validation and method verification 2.Which guidelines proposed to method transfer
In Dissolution Test why limit is define Q+5% what is the role of +5%.
What is the difference between purge septum flow and column flow in gas chromatography?
what is the principle of UV Vis spectroscopy, AAS, ICP OES,ICPAES, ICP-MS and FTIR
if identification threshold crosses the limits then what next step?