C. Altenstetter, US Perspectives on the EU Medical Device Approval System, and Lessons Learned from the United States, US Perspectives on the EU Medical Device Approval System, and Lessons Learned from the United States, pp.443-464, 2013.
DOI : 10.1056/NEJMp1114865

F. Cafaggi and A. Janczuk, Private Regulation and Legal Integration: The European Example, Business and Politics, vol.37, issue.03, 2010.
DOI : 10.1080/135017698343938

. Cetikm, The Business Forms and Controlling Shareholders of Notified Bodies " under The New Approach Regulation. A Preliminary Assessment to implement the Statute of, 2010.

N. Chowdhury and R. A. Wessel, Conceptualising Multilevel Regulation in the EU: A Legal Translation of Multilevel Governance?, European Law Journal, vol.18, issue.3, pp.335-357, 2012.
DOI : 10.1111/j.1468-0386.2012.00603.x

D. Cohen and M. Billingsley, Europeans are left to their own devices, Europeans are left to their own devices, p.2748, 2011.
DOI : 10.1136/bmj.d2748

URL : http://www.bmj.com/cgi/content/short/342/may13_2/d2748

M. Egan, Regulatory strategies, delegation and European market integration, Journal of European Public Policy, vol.5, issue.3, pp.485-506, 1998.
DOI : 10.1080/135017698343938

M. Egan, Constructing a European Market; Standards, regulation, and Governance, 52001.

C. Frankel and E. Höjbjerg, The constitution of a transnational policy field: negotiating the EU internal market for products, Journal of European Public Policy, vol.3, issue.1, pp.96-114, 2007.
DOI : 10.2307/3053986

J. Galland, The difficulties of Regulating Markets and Risks in Europe through Notified Bodies, European Journal of Risk Regulation, vol.4, issue.03, pp.365-373
DOI : 10.1111/j.1468-0491.2007.00344.x

URL : https://hal.archives-ouvertes.fr/hal-00927769

J. Galland, La difficile construction d'une expertise européenne indépendante. Le cas des organismes notifiés, Revue d, Anthropologie des Connaissances, vol.7, issue.1, pp.223-246

L. Hancher and M. E. Földes, Revision of the Regulatory Framework for Medical Devices in the European Union: The Legal Challenges, European Journal of Risk Regulation, vol.4, issue.04, pp.429-435, 2013.
DOI : 10.1017/S1867299X0000307X

D. Levi-faur and S. M. Starobin, Transnational politics and policy: from two-way to three-way interactions, 2014.

B. Lobmayr, An Assessment of the EU Approach to Medical Device Regulation against the Backdrop of the US System, European Journal of Risk Regulation, vol.16, issue.02, pp.137-149, 2010.
DOI : 10.1017/S1867299X00000222

. Locontoa and L. Busch, Standards, techno-economic networks, and playing fields: Performing the global market economy, Review of International Political Economy, vol.36, issue.3, pp.507-536, 2010.
DOI : 10.1111/1467-7679.00214

E. Previdi, The Organisation of Public and Private Responsibilities in European Risk Regulation: An Institutionnal Gap Between Them? in, Integrating Scientific Expertise into Regulatory Decision Making. National Traditions and European Innovations, 1997.

H. Schepel, The Constitution of Private Governance; Product Standards in the regulation of Integrating Markets, Oxford and Portland, 2005.

S. M. Singh, What is the Best Way to Supervise the Quality of Medical Devices? Searching for a Balance Between ex-ante and ex-post Regulation, European Journal of Risk Regulation, vol.13, issue.04, pp.465-477, 2013.
DOI : 10.1016/j.irle.2004.03.003