• Eur. J. Intern. Med. · Oct 2014

    Fostering EMA's transparency policy.

    • Rita Banzi, Vittorio Bertele', Jacques Demotes-Mainard, Silvio Garattini, Christian Gluud, Christine Kubiak, and Christian Ohmann.
    • IRCCS-Istituto di Ricerche Farmacologiche Mario Negri, via Giuseppe La Masa 19, 20156 Milano, Italy. Electronic address: rita.banzi@marionegri.it.
    • Eur. J. Intern. Med. 2014 Oct 1;25(8):681-4.

    AbstractThe European Medicines Agency has opened a window to access clinical trial data. This is an important step forward which deserves attention, support, and advice from all the stakeholders. Regulatory agencies are the most comprehensive repositories of clinical trial data on drugs and can also promote and develop standard practices for data sharing. The release of the EMA draft policy on publication and access to clinical trial data in 2013 has fueled a lively debate among academia, industry, and the public in general that is still ongoing. As clinical researchers and producers and users of clinical trial data, we endorse the European Medicines Agency's opening and offer a few suggestions for complete, safe, and effective data sharing.Copyright © 2014 European Federation of Internal Medicine. Published by Elsevier B.V. All rights reserved.

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