Interested to Buy Any Domain ? << Click Here >> for more details...
full name of OOS & OOT ? Dercribe it with details ? why
this is needed in pharma industry ?
- 10 Answers
- 38808 Views
- Orchid, I also Faced
- E-Mail Answers
Answer Posted / ramya
oos means out of specification.It is very useful for pharma industry because if any sample rejects the analyst should prepare an oos form.analyst should inform to supervisor and discuss the procedure what the analyst has followed. repetitions should be done based on company rules.
| Is This Answer Correct ? | 2 Yes | 3 No |
Post New Answer View All Answers
Why are use silicon oil mr?
Difference between hlaf and rlaf
why we use a particular hplc column for a particular compound give reasons?please
what is different when impergnated silica plates are used in separation of azo dyes using column chromatography?
how much mass should be there in volumetric flask while in preparation of sample for assay?
give clarity of linearity and range in method validation
[3/30, 13:29] Manoj P Venkatpurwar: How hplc column selection according to structure? How mobile phase buffer selection on molecule structure?
Why perchloric acid used for potentiometric titration
calibrtion procedue of LC-MS
If change in specification which parameter require to do for validation? if change in chromtographic condition then which parameter? if api change then which parameter? if change composition then which parameter? if old method not work out then whicj parameter? if additional one impurity added then which parameter of validation require to do on above each conditions? elaborate separately
In the HPLC Calibration done wavelength accuracy done between 200nm-280nm .but not done remaining 300-400nm not done ?
mahagenco syllabus for the post of chemist
Which type of column should i use to check the purity of high molecular weight protein using HPLC reverse phase column chromatography? Hi everyone. I wanna to check the purity of high molecular weight protein (collagen) with MW of ~130 kDa using a HPLC. I know C18
How do we get end points and how many end points are possible for citric acid and di-acid not theorotically answer should be given practically.
how you start the solubility study?
