CANCERSCREEN SIGNED
Screening for cancer in the post-genomic era: diagnostic innovation and biomedicalisation in comparative perspective
Total Cost €
0EC-Contrib. €
0Partnership
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0CANCERSCREEN project word cloud
Explore the words cloud of the CANCERSCREEN project. It provides you a very rough idea of what is the project "CANCERSCREEN" about.
Project "CANCERSCREEN" data sheet
The following table provides information about the project.
| Coordinator |
THE CHANCELLOR MASTERS AND SCHOLARSOF THE UNIVERSITY OF CAMBRIDGE
Organization address contact info |
| Coordinator Country | United Kingdom [UK] |
| Total cost | 1˙347˙992 € |
| EC max contribution | 1˙347˙992 € (100%) |
| Programme |
1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC)) |
| Code Call | ERC-2016-STG |
| Funding Scheme | ERC-STG |
| Starting year | 2017 |
| Duration (year-month-day) | from 2017-04-01 to 2021-09-30 |
Partnership
Take a look of project's partnership.
| # | ||||
|---|---|---|---|---|
| 1 | THE CHANCELLOR MASTERS AND SCHOLARSOF THE UNIVERSITY OF CAMBRIDGE | UK (CAMBRIDGE) | coordinator | 1˙047˙674.00 |
| 2 | THE UNIVERSITY OF SUSSEX | UK (BRIGHTON) | participant | 300˙317.00 |
Map
Project objective
Cancer screening and the diagnostics industry: a comparative analysis of the political economy of diagnostic innovation A decade after the Human Genome Project, major public and private investments continue to fuel expectations of a genomic revolution in biomedicine. The freight of expectations surrounding the new “age of diagnostics” is accompanied by much uncertainty about how public policy should steer diagnostic innovation, with much debate about inter alia the harms of creating diagnostic monopolies through gene patenting, and the risks of under- or over-regulation. However, due to the paucity of research on diagnostic innovation, policy deliberation is driven more by anecdote and expert opinion than empirical evidence. With a specific focus on screening/early detection of cancer, this project will map industry dynamics, technological trajectories and regulatory developments in Europe and the USA from 1996 to the present day. Combining quantitative and qualitative methods, the project’s innovative dimensions include a new conceptual model of socio-technical transition in the diagnostics sector, and the first integrative analysis linking scientometric data on the interactions between public and private actors in the diagnostic research domain with comparative transnational analysis of regulatory decision-making. Through a novel integration of conceptual insights from the literature on biomedicalisation and scholarship on socio-technical regime change, this project aims to advance both fields of research by applying a new multi-scale, multi-level model of socio-technical transition. The project will provide unprecedented insight into the factors shaping the development of a new generation of molecular diagnostic tests, and examine how these technologies are reconfiguring disease categories and redrawing the boundaries between health and sickness. We will establish a platform of theory and methods for a broader programme of work on diagnostic innovation.
Publications
| year | authors and title | journal | last update |
|---|---|---|---|
| 2019 |
Kelly Holloway, Fiona A Miller, Alberto Gutierrez, Stuart Hogarth Dangerous diagnostics? Regulatory reform in the genomic era published pages: l640, ISSN: 0959-8138, DOI: 10.1136/bmj.l640 |
BMJ | 2020-01-30 |
| 2019 |
Kelly Holloway, Fiona A. Miller, François Rousseau, Alberto Gutierrez, Stuart Hogarth Health Canada needs to act on laboratory-developed diagnostics published pages: E1067-E1069, ISSN: 0820-3946, DOI: 10.1503/cmaj.190550 |
Canadian Medical Association Journal 191/39 | 2020-01-30 |
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