what is mean by dissolution biowaiver study?
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in api coa contains only process impurities and in product coa contains degradation impurities?
Why Peak Purity is not determined in GC analysis?
why a ph meter require KCL solution for their storing condition?
In pharmaceuticals formulation OOS applicable in Raw Material(which is not manufacturing in the company. and purchase by approved vendor)).Why?
why we are using in ph calibrations ph4,7,9.2 buffers only?
How require to develop GC method? how to select diluent, GAS, column selection and other chromatographic conditions?
why should we perform dissolution PVT calibration only by UV spectrometer, not by HPLC ?
what is rt and rrt? how we find rrt? relation between rt and rrt/
what is mean by Q in S1 and S2
which lights using during force degradation?
How do you increase the number of theoretical plates?
what is MCG dilution in HPLC & GC analysis
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