why using factor 1.00639 in burette calibration of kf
1.00639 is water wt/ml at 25°c according to IP.
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At what distance the sample is collected in dissolution basket?
How to study genotoxicity of impurities in API?
how we can identify the impurity is coming below loq at transfering site?
How to select Sample concentration in RS analysis?example.
on what basis SOP's can be changed? IF mobile phase ratio is 70:30 to how much % can we change the ratio in HPLC process
For Recent draft guidelines for Dissolution test apparatus calibration, why removing the salicylate tables?
In performance Check of GC Why Hexadecane Peak is Considered
0 Answers Asian Paints, MSN Pharma,
How can I develope method of dissolution by HPLC OR UV
what is a differance between assay by HPLC and assay by titration?
in dissolution why pool sample needed? in which type of drug pool sample need?
How do we fix the sample concentaryion in hplc method development. What is the basis?
Chromatographic Purity is a Qualitative analysis