Produktdetaljer
Biografisk notat
Frederick M. Abbott, Edward Ball Eminent Scholar Professor of International Law, Florida State University College of Law, USA<i>‘This outstanding book provides comprehensive coverage of pharmaceutical law. It is an invaluable read for anyone seeking to understand the pharmaceutical ecosystem. The book also provides a robust foundation for those entering emerging or quickly shifting areas of the law, including artificial intelligence and telemedicine.’</i>
- Ana Santos Rutschman, Villanova University, USA,
<i>‘Professor Abbott’s important book fills a gap in the scholarly literature on pharmaceutical law. It offers an insightful general introduction to a complex and highly technical field of law, covering a broad range of topics with a rigorous analytical approach coupled with an accessible style fit for all audiences.’</i>
- Gian Luca Burci, Geneva Graduate Institute, Switzerland,
<i>‘In this concise, up-to-date and forward-looking book, Fred Abbott provides a comprehensive yet critical survey of the complex legal issues involved in pharmaceutical development and regulation. The book draws on his decades-long experience as one of the world's foremost experts in international intellectual property law and global health policy. A tour de force and an indispensable guide!’</i>
- Peter K. Yu, Texas A&M University, USA,
This Advanced Introduction provides a succinct overview of the vital role of pharmaceuticals in protecting and enhancing life and health. Frederick Abbott examines the global network of researchers and industrial companies involved in the developmental process, from fundamental research to testing, manufacturing and distribution. He evaluates the legal frameworks intended to promote the research and development of these essential medicines, including the use of patents, subsidies and other incentives.
Key Features:
- Addresses how the interests of diverse stakeholders are reconciled
- Discusses the use of technology licensing and the impact of AI on pharmaceutical IP
- Identifies the regulatory frameworks that ensure the safety and efficacy of therapeutic medicines and vaccines
- Analyses the broad range of pharmaceutical advertising, promotion and prescription, with a particular focus on the growing role of telemedicine
- Explores burgeoning global topics such as the implications of the USA’s withdrawal from the WHO and the emergence of China as a center for pharmaceutical research, development and patenting
Providing an accessible overview of the complex field of pharmaceutical regulation, this book is a necessary resource for scholars and students of health and biotechnology law. It is also beneficial for practitioners and policymakers in intellectual property law and pharmaceutical law.