Interested to Buy Any Domain ? << Click Here >> for more details...
On which pharmacopoeia basis we can calibrate instruments
like HPLC,GC,UV,DISSO,IR etc...
- 9 Answers
- 25335 Views
- Cipla, Laurus, Micro Labs, I also Faced
- E-Mail Answers
Answer Posted / narendra
IR Calibration as per EP
HPLC And GC Calibration are based on manifacture Suggest
| Is This Answer Correct ? | 0 Yes | 1 No |
Post New Answer View All Answers
What is importance of pH in the Heavy metal test and How it effect on the test results?
Explain the relations between number of carbon atoms in alkanes and retention time ?
what is lod and loq ?,why use k2cr2o7 , kcl h2so4 in uv calibration ?,why use benzophenone & caffene acetone in hplc calibration ?,what is leading peak in hplc ?why we do the calibration of limit of stry light in hplc & uv ?
In the isomers,enantiomers give the only physical properties present such that no chemical properties present.
how to get accurate result for Residue on evaporation in purified water
My question about gas chromatography sulfur chemiluminsecence detector. I test unknown sample gas by GC-SCD (calibrated ) and the result of *H2S is 279 PPM , *but when I test the same sample with the GC-TCD (calibrated ) the value of *H2S is 2500 PPM . I'd like to inform you that both GCs are calibrated and have very good operation conditions with stable parameters . the question is if the sample gas with higher H2S over detection limits of SCD detector (1000 ppm). why the result it 279 ppm Best regards
How require to perform linearity as per ANVISA? What are the acceptance criteria?
for which product require to do content uniformity? what is limit of cu?
what is third integration
what is mean by dissolution hydrodynamics?
if peak get problamatic then what require to do?
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
What is the diference between residual solvents and organic volatile matter
analytical method validation require to with respect to release specification or shelf life specification?
which are the sizes of capsules?
