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1.
Trends Biotechnol ; 35(8): 682-686, 2017 08.
Article in English | MEDLINE | ID: mdl-28487123

ABSTRACT

Government policies across the world seek to create clusters of companies and other stakeholders that specialise in a particular technology to build an 'industrial ecosystem'. This article looks at some examples of clusters created specifically with industrial biotechnology in mind and examines measures for policymakers.


Subject(s)
Biotechnology/economics , Biotechnology/legislation & jurisprudence , Biotechnology/trends , Public Sector , Humans
2.
Soc Stud Sci ; 47(1): 7-32, 2017 02.
Article in English | MEDLINE | ID: mdl-28195029

ABSTRACT

While there is ample scholarly work on regulatory science within the state, or single-sited global institutions, there is less on its operation within complex modes of global governance that are decentered, overlapping, multi-sectorial and multi-leveled. Using a co-productionist framework, this study identifies 'epistemic jurisdiction' - the power to produce or warrant technical knowledge for a given political community, topical arena or geographical territory - as a central problem for regulatory science in complex governance. We explore these dynamics in the arena of global sustainability standards for biofuels. We select three institutional fora as sites of inquiry: the European Union's Renewable Energy Directive, the Roundtable on Sustainable Biomaterials, and the International Organization for Standardization. These cases allow us to analyze how the co-production of sustainability science responds to problems of epistemic jurisdiction in the global regulatory order. First, different problems of epistemic jurisdiction beset different standard-setting bodies, and these problems shape both the content of regulatory science and the procedures designed to make it authoritative. Second, in order to produce global regulatory science, technical bodies must manage an array of conflicting imperatives - including scientific virtue, due process and the need to recruit adoptees to perpetuate the standard. At different levels of governance, standard drafters struggle to balance loyalties to country, to company or constituency and to the larger project of internationalization. Confronted with these sometimes conflicting pressures, actors across the standards system quite self-consciously maneuver to build or retain authority for their forum through a combination of scientific adjustment and political negotiation. Third, the evidentiary demands of regulatory science in global administrative spaces are deeply affected by 1) a market for standards, in which firms and states can choose the cheapest sustainability certification, and 2) the international trade regime, in which the long shadow of WTO law exerts a powerful disciplining function.


Subject(s)
Biofuels/standards , Government Regulation , International Cooperation , European Union , Organizations
4.
Neuron ; 92(3): 642-646, 2016 Nov 02.
Article in English | MEDLINE | ID: mdl-27810009

ABSTRACT

Technological advances have the potential to dramatically increase our understanding of the human brain, treat and cure injury and disease, and enhance our general well-being. While advances in neuroscience hold great promise, they also raise profound ethical, legal, and social questions. In this vein, the Organization for Economic Co-operation and Development (OECD) convened an international workshop in September 2016 to explore responsible research and innovation in brain science.


Subject(s)
Inventions/ethics , Neurosciences/ethics , Neurosciences/legislation & jurisprudence , Humans , Inventions/legislation & jurisprudence , Social Responsibility
6.
Soc Sci Med ; 73(3): 367-74, 2011 Aug.
Article in English | MEDLINE | ID: mdl-21726926

ABSTRACT

Biobanks are increasingly hailed as powerful tools to advance health research. The social and ethical challenges associated with the implementation and operation of biobanks are equally well-documented. One of the proposed solutions to these challenges involves trading off a reduction in the specificity of informed consent protocols with an increased emphasis on governance. However, little work has gone into formulating what such governance might look like. In this paper, we suggest four general principles that should inform biobank governance and illustrate the enactment of these principles in a proposed governance model for a particular population-scale biobank, the British Columbia (BC) Generations Project. We begin by outlining four principles that we see as necessary for informing sustainable and effective governance of biobanks: (1) recognition of research participants and publics as a collective body, (2) trustworthiness, (3) adaptive management, and (4) fit between the nature of a particular biobank and the specific structural elements of governance adopted. Using the BC Generations Project as a case study, we then offer as a working model for further discussion the outlines of a proposed governance structure enacting these principles. Ultimately, our goal is to design an adaptive governance approach that can protect participant interests as well as promote effective translational health sciences.


Subject(s)
Databases, Genetic , Genome , British Columbia , Community Participation , Genetic Research/ethics , Humans , Informed Consent , Trust
7.
Science ; 331(6018): 725-7, 2011 Feb 11.
Article in English | MEDLINE | ID: mdl-21311015

ABSTRACT

Many fields have struggled to develop strategies, policies, or structures to optimally manage data, materials, and intellectual property rights (IPRs). There is growing recognition that the field of stem cell science, in part because of its complex IPRs landscape and the importance of cell line collections, may require collective action to facilitate basic and translational research. Access to pluripotent stem cell lines and the information associated with them is critical to the progress of stem cell science, but simple notions of access are substantially complicated by shifting boundaries between what is considered information versus material, person versus artifact, and private property versus the public domain.


Subject(s)
Access to Information , Intellectual Property , Ownership , Stem Cell Research , Stem Cells , Biological Specimen Banks , Confidentiality , Humans , Informed Consent , Public Sector , Tissue Donors
8.
Stem Cell Rev Rep ; 5(2): 82-8, 2009 Jun.
Article in English | MEDLINE | ID: mdl-19521798

ABSTRACT

Few areas of recent research have received as much focus or generated as much excitement and debate as stem cell research. Hope for the therapeutic promise of this field has been matched by social concern associated largely with the sources of stem cells and their uses. This interplay between promise and controversy has contributed to the enormous variation that exists among the environments in which stem cell research is conducted throughout the world. This variation is layered upon intra-jurisdictional policies that are also often complex and in flux, resulting in what we term a 'patchwork of patchworks'. This patchwork of patchworks and its implications will become increasingly important as we enter this new era of stem cell research. The current progression towards translational and clinical research among international collaborators serves as a catalyst for identifying potential policy conflict and makes it imperative to address jurisdictional variability in stem cell research environments. The existing patchworks seen in contemporary stem cell research environments provide a valuable opportunity to consider how variations in regulations and policies across and within jurisdictions influence research efficiencies and directions. In one sense, the stem cell research context can be viewed as a living experiment occurring across the globe. The lessons to be gleaned from examining this field have great potential for broad-ranging general science policy application.


Subject(s)
Embryo Research , Stem Cells , Animals , Embryo Research/ethics , Embryo Research/legislation & jurisprudence , Humans
11.
J Law Med Ethics ; 35(3): 440-56, 2007.
Article in English | MEDLINE | ID: mdl-17714253

ABSTRACT

A property analysis of the U.K. Biobank reveals a new imagination of the genomic biobank as a national common-pool resource. U.K. Biobank's treatment of property and governance exhibit both strengths and weaknesses that may be instructive to genome project planners around the world.


Subject(s)
Biological Specimen Banks/organization & administration , Community-Institutional Relations , Databases, Genetic/legislation & jurisprudence , Genome, Human , Ownership/legislation & jurisprudence , Tissue Donors/legislation & jurisprudence , Adult , Aged , Biological Specimen Banks/ethics , Biological Specimen Banks/legislation & jurisprudence , Databases, Genetic/ethics , Genetic Research , Genome, Human/ethics , Humans , Middle Aged , Models, Organizational , Ownership/ethics , Politics , Tissue Donors/ethics , United Kingdom
12.
Trends Biotechnol ; 24(9): 390-4, 2006 Sep.
Article in English | MEDLINE | ID: mdl-16843559

ABSTRACT

Owing to the restrictive human embryonic stem cell (hESC) policies of the US government, the question of whether to pursue human embryonic stem cell experiments has dominated the ethical and political discourse concerning such research. Explicit attention must now turn to problems of implementing the research on a large scale: in the 2004 US elections, California voters approved a state initiative for stem cell research, earmarking $3 billion in direct spending over 10 years. This article explores three ethical and political problem areas emerging out of the California program, the resolution of which will help set the trajectory of hESC research in the US and abroad, and then proposes an institutional approach to help address them: a network of public stem cell banks in the US that feature transparent and shared governance.


Subject(s)
Embryo Research/legislation & jurisprudence , Financing, Government/legislation & jurisprudence , Oocyte Donation/standards , Research Support as Topic/legislation & jurisprudence , California , Embryo Research/economics , Financing, Government/economics , Financing, Government/organization & administration , Humans , Intellectual Property , Oocyte Donation/economics , Public Policy , Research Support as Topic/economics , Research Support as Topic/organization & administration , State Government , Stem Cells , Tissue Banks/economics , Tissue Banks/legislation & jurisprudence , Tissue Banks/organization & administration , United States
15.
Jurimetrics ; 43(2): 187-228, 2003.
Article in English | MEDLINE | ID: mdl-15156881

ABSTRACT

Existing scholarship on population genomics has only superficially addressed issues of power and political process. Accordingly, questions of politics and governance pervade the analysis of three population genomics case studies that follow: the Human Genome Diversity Project, Iceland's Health Sector Database, and "Clinical Genomics" as defined by the Beth Israel-Ardais collaboration. An examination of these case studies reveals that the common law, U.S. regulatory law, and international law have not developed the political sophistication to make the traditional promises of biomedical ethics--respect for autonomy, justice, and beneficence--come to fruition. Further, comparisons of these projects illuminate three areas ripe for reframing--informed consent, expert ethical oversight, and commercial benefits. Four avenues of reform are suggested.


Subject(s)
Databases, Nucleic Acid/ethics , Databases, Nucleic Acid/legislation & jurisprudence , Ethical Review , Genetic Research/ethics , Genetic Research/legislation & jurisprudence , Genetics, Population/ethics , Genetics, Population/legislation & jurisprudence , Internationality , Politics , Private Sector , Public Sector , Advisory Committees , Beneficence , Bioethics , Blood Specimen Collection/ethics , Commodification , Conflict of Interest , Decision Making , Ethics Committees, Research , Genetic Privacy , Government Regulation , Human Experimentation/legislation & jurisprudence , Human Genome Project , Human Rights/legislation & jurisprudence , Humans , Iceland , Industry , Informed Consent , Medical Records , Patents as Topic , Personal Autonomy , Presumed Consent , Racial Groups/genetics , Research Subjects , Risk Assessment , Social Justice , Tissue Banks/ethics , Tissue Banks/legislation & jurisprudence , Tissue Donors , United States
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