Can research ethics committees enable clinical trial data sharing

[1]  Iris Pigeot,et al.  Consent and confidentiality in the light of recent demands for data sharing , 2017, Biometrical journal. Biometrische Zeitschrift.

[2]  Francis S. Collins,et al.  The 21st Century Cures Act - A View from the NIH. , 2017, The New England journal of medicine.

[3]  Rieke van der Graaf,et al.  International Ethical Guidelines for Health-related Research involving Humans , 2017 .

[4]  B. Knoppers,et al.  Ethics review for international data-intensive research , 2016, Science.

[5]  Erik Schultes,et al.  The FAIR Guiding Principles for scientific data management and stewardship , 2016, Scientific Data.

[6]  Y. Joly,et al.  Locating Biobanks in the Canadian Privacy Maze , 2016, Journal of Law, Medicine & Ethics.

[7]  John Fletcher,et al.  Sharing Clinical Trial Data: A Proposal from the International Committee of Medical Journal Editors , 2016, The National medical journal of India.

[8]  Jordi Rambla De Argila,et al.  Consent Codes: Upholding Standard Data Use Conditions , 2016, PLoS genetics.

[9]  Y. Joly,et al.  Protecting the Privacy of Canadians’ Health Information in the Cloud , 2016 .

[10]  B. Knoppers,et al.  Harmonizing Privacy Laws to Enable International Biobank Research , 2015, Journal of Law, Medicine & Ethics.

[11]  S. Bull,et al.  Views of Ethical Best Practices in Sharing Individual-Level Data From Medical and Public Health Research , 2015, Journal of empirical research on human research ethics : JERHRE.

[12]  B. Lo.  Sharing clinical trial data: maximizing benefits, minimizing risk. , 2015, JAMA.

[13]  Jeffrey M Drazen,et al.  Sharing individual patient data from clinical trials. , 2015, The New England journal of medicine.

[14]  Michael Morrison,et al.  Dynamic consent: a patient interface for twenty-first century research networks , 2014, European Journal of Human Genetics.

[15]  Bartha M. Knoppers,et al.  Data sharing, year 1--access to data from industry-sponsored clinical trials. , 2014, The New England journal of medicine.

[16]  Bartha Maria Knoppers,et al.  Framework for responsible sharing of genomic and health-related data , 2014, The HUGO Journal.

[17]  Oliver Butters,et al.  DataSHIELD: taking the analysis to the data, not the data to the analysis , 2014, International journal of epidemiology.

[18]  Mark Barnes,et al.  Preparing for responsible sharing of clinical trial data. , 2013, The New England journal of medicine.

[19]  Y. Khaliq,et al.  Tri-Council Policy Statement: Ethical Conduct for Research Involving Humans , 2012 .

[20]  Peter C Gøtzsche,et al.  Why we need easy access to all data from all clinical trials and how to accomplish it , 2011, Trials.

[21]  Kevin M Gowdie.  Privacy and security policy , 2011 .

[22]  D. Altman,et al.  Towards agreement on best practice for publishing raw clinical trial data , 2009, Trials.

[23]  Eric Puybaret,et al.  Universal Declaration of Human Rights , 2006 .

[24]  H. Mann.  Research ethics committees and public dissemination of clinical trial results , 2002, The Lancet.

[25]  Robert Kevin Grigsby,et al.  Federal Policy for the Protection of Human Subjects , 1993, Research on social work practice.

[26]  Bandman El.  Protection of human subjects. , 1980, JAMA.