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Regulation of Genome Editing in Human iPS Cells

ISBN-13: 9783030930257 / Angielski / Miękka / 2023

Regulation of Genome Editing in Human iPS Cells  9783030930257 Springer International Publishing - książkaWidoczna okładka, to zdjęcie poglądowe, a rzeczywista szata graficzna może różnić się od prezentowanej.

Regulation of Genome Editing in Human iPS Cells

ISBN-13: 9783030930257 / Angielski / Miękka / 2023

cena 645,58 zł
(netto: 614,84 VAT:  5%)

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The book provides a concise overview of currently applicable regulatory frameworks of states which are among the world leaders in research and development (R&D) of cell and gene therapies. Developments in genome editing are expected to lead to new possibilities for the treatment of hereditary diseases in humans. The treatment of such often severe but hitherto uncurable diseases can be based on genome-edited induced pluripotent stem cells (iPS cells). Such treatments constitute combined cell/gene therapies. These therapies need to be governed by a regulatory framework which ensures quality, safety, and efficacy of the relevant therapeutic products. On the other hand, such regulations may retard product approval and impede R&D. Accordingly, national regulations for therapies based on genome-edited iPS cells are an important and, as the case may be, decisive factor for both researchers and industry regarding their decision where to locate their R&D activities. Therefore, regulatory frameworks impact significantly on the competitiveness of states and their economies. This is why a comparative analysis of laws and regulations of different countries matters. Such a comparative legal analysis provides an important insight into regulatory concepts which, in turn, may inspire adjustments of, or amendments to, domestic legal regimes. For this purpose, experts present country reports on France, Germany, Japan, South Korea, Switzerland, and the USA. The reports on France and Germany also refer to the parameters and implications arising from pertinent EU law. This contributed volume is aimed at researchers, but also at, e.g., legal scholars, lawmakers, regulators, and political decision makers.

Kategorie:
Nauka, Prawo i administracja
Kategorie BISAC:
Law > International
Medical > Genetyka kliniczna
Law > Comparative
Wydawca:
Springer International Publishing
Język:
Angielski
ISBN-13:
9783030930257
Rok wydania:
2023
Waga:
0.53 kg
Wymiary:
23.5 x 15.5
Oprawa:
Miękka
Dodatkowe informacje:
Wydanie ilustrowane

Introduction.- Biological Aspects of Genome Editing in iPS Cells.- Ethical Aspects in the Context of Genome Editing.- Regulation of Genome Editing in iPS Cells: Germany.- Regulation of Genome Editing in iPS Cells: France.- Regulation of Genome Editing in iPS Cells: Switzerland.- Regulation of Genome Editing in iPS Cells: United States.- Regulation of Genome Editing in iPS Cells: Japan.- Regulation of Genome Editing in iPS Cells: Republic of Korea.- Comparative Analysis.

Hans-Georg Dederer is a full professor and holder of the Chair of Constitutional and Administrative Law, Public International Law, European and International Economic Law at the University of Passau (Germany). His fields of research include biotechnology law. He is also a member of the Permanent Senate Commission on Genetic Research of the German Research Foundation (Deutsche Forschungsgemeinschaft – DFG).

Gregor Frenken is a teaching and research assistant in the Chair of Constitutional and Administrative Law, Public International Law, European and International Economic Law at the University of Passau (Germany).

The book provides a concise overview of currently applicable regulatory frameworks of states which are among the world leaders in research and development (R&D) of cell and gene therapies. Developments in genome editing are expected to lead to new possibilities for the treatment of hereditary diseases in humans. The treatment of such often severe but hitherto uncurable diseases can be based on genome-edited induced pluripotent stem cells (iPS cells). Such treatments constitute combined cell/gene therapies. These therapies need to be governed by a regulatory framework which ensures quality, safety, and efficacy of the relevant therapeutic products. On the other hand, such regulations may retard product approval and impede R&D. Accordingly, national regulations for therapies based on genome-edited iPS cells are an important and, as the case may be, decisive factor for both researchers and industry regarding their decision where to locate their R&D activities. Therefore, regulatory frameworks impact significantly on the competitiveness of states and their economies. This is why a comparative analysis of laws and regulations of different countries matters. Such a comparative legal analysis provides an important insight into regulatory concepts which, in turn, may inspire adjustments of, or amendments to, domestic legal regimes. For this purpose, experts present country reports on France, Germany, Japan, South Korea, Switzerland, and the USA. The reports on France and Germany also refer to the parameters and implications arising from pertinent EU law. This contributed volume is aimed at researchers, but also at, e.g., legal scholars, lawmakers, regulators, and political decision makers.



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