Abstract
A range of analytical techniques can be used to prove that the structural integrity of an active pharmaceutical biological ingredient has been retained following any necessary purification. These analyses should assess the intactness, protein backbone, PTMs, oligosaccharide profile and secondary/tertiary structure of the product, pre- and post-purification.
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CITATION STYLE
APA
Morris, H., & Reason, A. (2015). Compare and contrast. EBR - European Biopharmaceutical Review, (October), 18–24. https://doi.org/10.7748/ns.24.38.62.s52
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