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The International Conference of Harmonization (ICH) has worked on har- nizing the stability regulations in the US, Europe, and Japan since the early 1990s. Even though the Stability Guidelines Q1A (R2) was issued over a decade ago, issues surrounding this arena continue to surface as the principles described in the guideline are applied to different technical concentrations. As a result, the stability community has continued to discuss concerns and find ways of harmonizing regulatory requirements, streamlining practices, improving processes in order to bring safe and effective medical supplies to the patients around the world. In 2007, the American Association of Pharmaceutical Scientists (AAPS) Stability Focus Group organized two workshops – the Stability Workshop and the Degradation Mechanism Workshop. These meetings attracted many industry scientists as well as representatives from several regulatory agencies in the world to discuss important topics related to pharmaceutical stability practices. Recognizing the importance of documenting these discussions and with the permission of AAPS, I have worked with speakers to assemble a collection of 30 articles from presentations given at these two meetings, mainly the Stability Workshop. I trust that this book will be beneficial to all of you in providing guidance and up-to-date information for building quality stability programs. v Freedom of our mind is Mother of all inventions.
The book addresses the ongoing challenges and evolving practices in pharmaceutical stability testing required to meet global regulatory standards. Authored by Kim Huynh-Ba, this work compiles articles from AAPS workshops, focusing on harmonizing stability regulations across the US, Europe, and Japan. It delves into the practical application of ICH guidelines, particularly Q1A(R2), and explores concerns that arise when these principles are applied to various technical concentrations. The book aims to provide industry scientists and regulatory representatives with up-to-date information and guidance for developing robust quality stability programs, ultimately ensuring safe and effective medical supplies reach patients worldwide.
This compilation, drawing from AAPS workshops, offers a focused perspective on the critical field of pharmaceutical stability testing. The content is geared towards industry scientists and regulatory professionals grappling with the complexities of global harmonization. The book's strength lies in its practical approach, addressing real-world application challenges and providing guidance for robust stability programs. It serves as a valuable resource for those involved in ensuring the quality and safety of medical supplies for international markets.
Page Count:
266
Publication Date:
2010-05-06
Publisher:
Springer New York
ISBN-10:
1441908900
ISBN-13:
9781441908902
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