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Contact Details

Phone:

+44 (0)1223 339739

Fax:

+44 (0)1223 464217

Email:

ld308at symbolcam.ac.uk

NOTE: if copying this email you will need to re-insert the '@' symbol

Position

Research Associate

Affiliation

Laure Brévignon Dodin

Laure Brévignon-Dodin has been a Research Associate within the Centre for Industry and Government since September 2005. Her work focuses on investigating regulatory frameworks and designing regulatory options to assist in the emergence of new technologies and industries.

She has collaborated with several EPSRC programmes. She completed a project research as part of the REMEDI Grand Challenge which was concerned with understanding the conditions to support the emerging industry of regenerative medicine in the UK. She is currently exploring the regulatory environment for commercialisation of photonic and electronic based products for the Cambridge Integrated Knowledge Centre (CIKC) project. She is also involved with the Emerging Industries Programme wherein she is investigating how regulation impacts on innovation.

Prior to joining the University of Cambridge, Laure’s work experience was in politics. She worked in Paris as a government practitioner for the Minister of Health and as a representative for a parliamentary group at the French National Assembly. She also gave lectures in public law and supervised research work at the Sorbonne University for 10 years.

Her background is mostly legal with a postgraduate degree in EU law. She studied international law and politics at Trinity College, Dublin.

Laure is very fond of literature and in her spare time, she is a freelance reviewer of English/American novels and editorial advisor for a French publishing company. She also runs the book club at the Alliance Francaise of Cambridge.

Publications

Journal Papers

  • L. Brévignon-Dodin and P. Singh, ATMP in practice: toward a new industry landscape in tissue engineering, Journal of Commercial Biotechnology, Vol.1, No.15, 59-65, January 2009
  • L. Brévignon-Dodin and F. Livesey, What can be learnt from the Japanese regulatory approach to tissue engineered products?, Regenerative Medicine, Vol.2, No.6, 967-971, November 2007.
  • R. P. Kulkarni, F. Livesey and L. Brévignon-Dodin, Will regulation determine the science agenda? A look at human embryonic stem cells (hESC). Regenerative Medicine, Vol.2, No.5, 839-844, September 2007
  • L. Brévignon-Dodin and Finbarr Livesey, Regulation of tissue-engineered products in the European Union: where are we heading? Regenerative Medicine, Vol.1, No.5, 709-714, September 2006
  • L. Brévignon-Dodin, Regulatory enablers and regulatory challenges for the development of tissue-engineered products in the EU, International Journal of Bio-medical materials and Engineering, Vol.20, No 3-4, 121-126, November 2010
  • P. Singh, L. Brévignon-Dodin and S.P. Dash, Exploratory assessment of the current EU regulatory framework for the development of advanced therapies, Journal of Commercial Biotechnology, Vol.16, No.4, 331-336, October 2010

Conference Papers

  • L. Brévignon-Dodin. A review of the regulatory framework for regenerative medicine- based therapeutic products in the EU. Pôle Lorrain d'Ingénierie du Cartilage (PLIC) 4èmes Journées, Nancy, 4-5 Feb 2010.
  • Laure Brévignon-Dodin, Tissue-engineered products: conditions for a supportive regulatory environment, Stem Cells Europe Conference, Amsterdam, 1-3 September 2008

  • L. Brévignon-Dodin, The regulation of emerging healthcare technologies and the need for a renewed regulatory approach to gain public acceptance, 2nd Annual Cambridge Conference, Centre for Business Research (Judge Business School), September 2007

Working papers

  • Laure Brévignon-Dodin, Regulation as an enabler for emerging industries Literature review, CIG Working Paper 2009/2.
  • Laure Brévignon-Dodin, Exploring regulatory and standards strategies to support the development of advanced photovoltaics, CIG Working Paper 2009/1.
  • Finbarr Livesey, Anke Zimmermann, Laure Brévignon-Dodin, Mike Gregory. Enabling the emergence of the regenerative medicine industry in the UK, CIG Working Paper 2008/3.
  • Laure Brévignon-Dodin, TEPs: challenging aspects for the UK regulatory framework and policy environment, 2007
  • Laure Brévignon-Dodin, The regulation of TEPs in the EU and in the UK: a work in progress, 2007
  • Laure Brévignon-Dodin, Exploratory analysis of the EU and UK regulatory frameworks for RM products, 2006
  • Towards a practitioners’ perspective on standards, L. Brévignon-Dodin, CIG Working Paper 2010/2.

 


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