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Precision medicine: drowning in a regulatory soup?

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posted on 2025-05-11, 11:58 authored by Dianne Nicol, Tania Bubela, Margaret Otlowski, Nola M. Ries, Loane Skene, Cameron Stewart, Jennifer Wagner, Nik Zeps, Don Chalmers, Jan Charbonneau, Christine Critchley, Joanne Dickinson, Jennifer Fleming, Alex W. Hewitt, Johnathan Liddicoat, Rebekah McWhirter
As US President Barack Obama noted in his 2015 State of the Union address, precision medicine promises to deliver 'the right treatments, at the right time, every time to the right person' which 'gives us one of the greatest opportunities for new medical breakthroughs that we have ever seen'. These comments were a prelude to a $215 million funding commitment by the President to his Precision Medicine Initiative, the aim of which is to 'pioneer a new model of patient-powered research that promises to accelerate biomedical discoveries and provide clinicians with new tools, knowledge, and therapies to select which treatments will work best for which patients'. The objectives include an undertaking to modernize the current regulatory landscape.

Funding

ARC

DP110100694

History

Journal title

Journal of Law and the Biosciences

Volume

3

Issue

2

Pagination

281-303

Publisher

Oxford University Press

Language

  • en, English

College/Research Centre

Faculty of Business and Law

School

School of Law and Justice

Rights statement

© The Author 2016. Published by Oxford University Press on behalf of Duke University School of Law, Harvard Law School, Oxford University Press, and Stanford Law School. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

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