Which Pharmacopiea follow calibration of HPLC,GC
Answer Posted / sendhil k
Ep
| Is This Answer Correct ? | 8 Yes | 0 No |
Post New Answer View All Answers
If vendor having more imp than monograph then how to proceed? and how to set spec?
How do we fix the sample concentaryion in hplc method development?
Why only 1.2 million lux hours require in photostability study?
What is the difference between chromatographic purity and related substances?
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?
analytical method validation require to with respect to release specification or shelf life specification?
How to calculation of residual solvent methanol (3000 ppm) standard solution, and how many quantity used of test sample
In which situation we require to prepare the standard solution from sample in Related substance method?
How can the GC or HPLC method is selected to determine the impurity profile in drug product?
how you determine moist.of NaOH sol or NaOH flacks
what is mean by dissolution biowaiver study?
in which situation require to change rs specification?
USP methodology, EP methodology, IP methodology, among three if possible to use one methodology for qualify working standard to use USP, EP, IP ? Please explain...
How will u perform degradation study in detectors other thann PDA in HPLC Methodology
mode of absorption in alimentary canal?