Nested randomized trials in large cohorts and biobanks: studying the health effects of lifestyle factors, Epidemiology, vol.19, issue.1, pp.75-82, 2008. ,
The randomized registry trial--the next disruptive technology in clinical research?, N Engl J Med, vol.369, issue.17, pp.1579-81, 2013. ,
Sharing and Reuse of Individual Participant Data from Clinical Trials: Principles and Recommendations, BMJ Open, vol.7, issue.12, p.18647, 2017. ,
Big data and open data: what kind of access should researchers enjoy, Therapie, vol.71, issue.6, pp.107-121, 2016. ,
UE) 2016/679 du Parlement européen et du Conseil du 27 avril, 2016. ,
, Journal officiel de l'Union européenne. EUR-Lex
, Conseil relatif aux essais cliniques de médicaments à usage humain et abrogeant la directive 2001/20/CE. Avril, vol.158, 2014.
, Journal officiel de l'Union européenne
, Conseil du 5 avril 2017 relatif aux dispositifs médicaux, modifiant la directive 2001/83/CE, le règlement (CE), vol.178, 2002.
78-17 du 6 janvier 1978 relative à l'informatique, aux fichiers et aux libertés, 2018. ,
, Article 29 Newsroom -News overview -European Commission, 2018.
Broken promises of privacy: responding to the surprising failure of anonymization, UCLA Law Review, vol.57, issue.9, p.12, 2010. ,
Health data in an open world. Cornell university library, 2017. ,
, Publication of MBS/PBS Data -Office of the Australian information commissioner (OAIC), 2018.
K-anonymity: a model for protecting privacy, International Journal of Uncertainty, Fuzziness and Knowledge-Based Systems, vol.10, issue.5, pp.557-70, 2002. ,
Classification of Processes Involved in Sharing Individual Participant Data from Clinical Trials. Version 2. F1000Res, vol.7, p.138, 2018. ,
, Système national des données de santé. Septembre, 2018.
Rapport health data hub, 2018. ,
« The French CONSTANCES Population-Based Cohort: Design, Inclusion and Follow-Up », Eur J Epidemiol, vol.30, issue.12, pp.1317-1345, 2015. ,
,
Obesity and emergency care in the French CONSTANCES cohort, PLoS One, vol.13, issue.3, p.194831, 2018. ,
Sharing clinical trial data: a proposal from the International committee of medical journal editors, Lancet, vol.387, pp.1279-1288, 2016. ,
Data sharing statements for clinical trials: a requirement of the International committee of medical journal editors, PLoS Medicine, vol.14, issue.6, p.1002315, 2017. ,
Preparing Raw Clinical Data for Publication: Guidance for Journal Editors, Authors, and Peer Reviewers, Trials, vol.11, p.9, 2010. ,
Transparency and the European medicines agency--sharing of clinical trial data, N Engl J Med, vol.371, issue.26, pp.2452-2457, 2014. ,
Clinical trial participants' views of the risks and benefits of data sharing, N Engl J Med, vol.378, issue.23, pp.2202-2213, 2018. ,
Strategies for dealing with missing data in clinical trials: from design to analysis, Yale J Biol Med, vol.86, issue.3, pp.343-58, 2013. ,
Attractivité de la France pour la recherche clinique internationale : résultats de la 8è enquête du Leem, Therapie, vol.73, issue.5, pp.367-76, 2018. ,
, World health organization. International clinical trials registry platform. Primary registries, 2018.
, World health organization. International clinical trials registry platform. WHO data set, 2018.
GPRD code of conduct, 2018. ,