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Property Rights in Blood, Genes and Data

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Bovenberg, Jasper A. 作者
Brill Academic Pub
譯者
2005-12 出版日期
226 頁數
$ 107.35 價格
Pap
叢書系列
9789004150539 圖書編碼

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發表於2024-11-08

Property Rights in Blood, Genes and Data 在線電子書 epub 下載 mobi 下載 pdf 下載 txt 下載 2024

Property Rights in Blood, Genes and Data 在線電子書 epub 下載 pdf 下載 mobi 下載 txt 下載 2024

Property Rights in Blood, Genes and Data 在線電子書 pdf 下載 txt下載 epub 下載 mobi 下載 2024



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Property Rights in Blood, Genes and Data 在線電子書 圖書描述

Who owns our DNA? The intuitive answer to this question is readily apparent: you own your own DNA. However, since Watson and Crick discovered its molecular structure, our DNA has gradually evolved from the Secret of Life to a potentially lucrative Commodity. This development has triggered conflicting perspectives as to who holds legal title to our blood, genes and related health data. Rather than focusing on a specific property claim in isolation, this book is the first to provide an integrated analysis of the merits of each of these perspectives. While the United Nations have proclaimed human DNA as the Heritage of Humanity, industry claims it to be patentable subject matter. Whereas populations whose DNA is used in national biobanks claim their DNA as their National Property, individual patients increasingly stand up for their Personal Property Rights in their samples. Meanwhile academic researchers claim their collections of biological materials as their Academic Property. Taking a case and context driven approach and backing up traditional legal analysis with historical analogies, web-surveys and practical experience, Jasper Bovenberg provides counter-intuitive, provocative and practical answers and recommendations for such controversial issues as how to share the benefits of DNA research, whether or not to recognize personal property rights in bodily material and access to biomedical datasets in academia. This book will interest not only lawyers and researchers, but also universities, funding agencies, industry and policymakers worldwide. It is also written to inform patients, their relatives, doctors and anyone else with an interest in a dilemma that is as universal as our DNA.

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