On which pharmacopoeia basis we can calibrate instruments
like HPLC,GC,UV,DISSO,IR etc...
Answer Posted / sanjay kumar
As per requir ment we can calibrate instrument like as
HPLC,GC,UV & IR mainily calibrate as per indian pharmocopeia
Is This Answer Correct ? | 3 Yes | 4 No |
Post New Answer View All Answers
what is the principle of UV Vis spectroscopy, AAS, ICP OES,ICPAES, ICP-MS and FTIR
which are the sizes of capsules?
What is the acceptance criteria for moisture balance when calibrated with sodium sulfate
How we performed the force degradation for drug substance, is any specific guideline is available for each parameter(Acidic, basic, oxidation,heat)? what conditions you mentained for above parameters.
mode of absorption in alimentary canal?
in which situation ion pair require to use?
How require to develop GC method? how to select diluent, GAS, column selection and other chromatographic conditions?
in DMF having extra impurities and in api COA also having extra imp than USP or BP product then how require to proceed?
What is delay volume?
all types of questions asked at the cipla interview
In GC calibration,what is the procedure to calibrate the TCD (thermal counductivity detector)suggest ?
I have compare C2H2-air and C2H2-N2O flame AAS on determination calcium. Both use same range of std to plot calibration curve. (2-6ppm) When i measure the sample with phosphate, KCl and LaCl, C2H2-N2O flame give false positive result, around 0.5ppm. When i measure the sample with phosphste, KCl and EDTA. C2H2-N2O flame also give 0.5ppm false positive. But both above mentioned sample would not give false positive when measured by C2H2-air flame. What is the reason?
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
Which parameters require to do in tech transfer?
what is %labelled amount in content uniformity of dosage unit and its calculation?