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4. Describe the operation of the Craig apparatus. Chapter.3 Equilibrium Processes in Separations
could negative ions be produced by bombardment process in mass spectrometry?
What is a difference between potency and purity?
inhouse product is in capsule form in combination and RLD is in tablet form then can we proceed for multimedia CDP? in inhouse capsule product disso is paddle with sinker in release media is there then RLD product in tablet form then with same as paddle with sinker we can proceed n.a.?
sop of a uv visible spectrophotometer double beam elico model
what is mean by ambient temperature?
why we should take dst factor for below 1%moisture samples
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
what is procedure of actual procedure for registration of drug?
if instrument calibration fails then what require to do?
Why six unit used for precision?
In IR spectra, generally a molecule vibrates without apply emr or ir light?
why require to do water content for drug product?
in each media we require to use SLS? how to proceed?
If inhouse hplc related substance method is completly diffrent from Usp for finished proďuct with diffrent impurities then how require to prove method equivalecy?
