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  1. Illegality in the Research Protocol: The Duty of Research Ethics Committees under the 2001 Clinical Trials Directive.Christopher Roy-Toole - 2008 - Research Ethics 4 (3):111-116.
    In this paper, the author shows how research ethics committees must deal with illegality in the research protocol. He defines their legal duty by reference to the 2001 Clinical Trials Directive, and especially in the key areas of insurance, indemnity and no-fault compensation. The author is critical of the current GAfREC and recent guidelines issued by the Royal College of Physicians. He concludes that new rules are needed to replace the 2001 edition of GAfREC.
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  • Research Ethics Committees and the Legality of the Protocol: A Rejoinder and a Challenge to the Department of Health.Christopher Roy-Toole - 2009 - Research Ethics 5 (1):33-36.
    This article is a response to the letter from the Department of Health that was published in the previous edition of the Research Ethics Review upon the matter of the legal duty of the research ethics committees. It also deals briefly with the article published in the current edition of Research Ethics Review by Colin Parker on what appears to be the same topic.
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  • Meeting the Needs of the Investigator and the REC Member.John Saunders - 2007 - Research Ethics 3 (4):111-112.
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  • The Legal Research Committee: A Response to Roy-Toole.Colin Parker - 2009 - Research Ethics 5 (1):30-32.
    The role of the REC is to aim for a fair and effective trial protocol and to provide to potential trial subjects sufficient information to allow them to make a rational decision on whether to participate in it or not. The members are medical specialists and members of the public together fitted to these tasks. In his paper ‘Illegality in the research protocol: the duty of research ethics committees under the 2001 Clinical Trials Directive’ Roy-Toole has made a number of (...)
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  • GAfREC Harmonised, NRES Rules.Roger Rawbone - 2009 - Research Ethics 5 (3):89-90.
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