Abstract
In biopharmaceutical productions field the purification proces is a crucial step in order to obtain Drugs whit impurity profile according the regulatory agency requirement. Aim of this work is to verify some relevant and recent literature and after analysis to submit to the researcher new Solutions in order to improve the global safety and the toxicological profile: is submitted a project related the in continuous testing of the purified materials using Raman spectroscopy - with pretreatment of the sample.
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