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Answer Posted / beesetty
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what are risk assement in the analytical qbd?
What if impurity area in control sample coming more as compared to LOQ level of impurity ?
how you confirm the assay method?
how many types of balance calibration test?
How can the GC or HPLC method is selected to determine the impurity profile in drug product?
how to qualify the impurity?
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?
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
Why perchloric acid used for potentiometric titration
what is mean by nitrosamine impurities?
why salisylic acid not using now days for disdolution calibration?
What is delay volume?
In the HPLC Calibration done wavelength accuracy done between 200nm-280nm .but not done remaining 300-400nm not done ?
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.?
how can I make the copper get white bye any salt or acit?
