Author(s): Alsante KM, Ando A, Brown R, Ensing J, Hatajik TD,
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Abstract Forced degradation studies are used to facilitate the development of analytical methodology, to gain a better understanding of active pharmaceutical ingredient (API) and drug product (DP) stability, and to provide information about degradation pathways and degradation products. In order to fulfill development and regulatory needs, this publication provides a roadmap for when and how to perform studies, helpful tools in designing rugged scientific studies, and guidance on how to record and communicate results.
This article was published in Adv Drug Deliv Rev
and referenced in Journal of Bioequivalence & Bioavailability