Abstract
The purpose of this chapter is introducing the goal of stability testing and its role in the Drug Development Process. It gives a brief overview of how stability studies are designed to support the development and commercialization of a new medicine. This chapter also acquaints the reader to the content of this book.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
Similar content being viewed by others
References
ICH Harmonized tripartite guidelines for stability testing of new drug substances and products – Q1A(R2)
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2009 Springer Science+Business Media, LLC
About this chapter
Cite this chapter
Huynh-Ba, K. (2009). Introduction. In: Huynh-Ba, K. (eds) Handbook of Stability Testing in Pharmaceutical Development. Springer, New York, NY. https://doi.org/10.1007/978-0-387-85627-8_1
Download citation
DOI: https://doi.org/10.1007/978-0-387-85627-8_1
Publisher Name: Springer, New York, NY
Print ISBN: 978-0-387-85626-1
Online ISBN: 978-0-387-85627-8
eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)