Ethics and observational studies in medical research: various rules in a common framework
Author(s) -
Frédérique Claudot,
François Alla,
Jeanne Fresson,
Thierry Calvez,
H. Coudane,
Catherine BonaïtiPellié
Publication year - 2009
Publication title -
international journal of epidemiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.406
H-Index - 208
eISSN - 1464-3685
pISSN - 0300-5771
DOI - 10.1093/ije/dyp164
Subject(s) - observational study , legislation , standardization , research ethics , institutional review board , modalities , harmonization , political science , engineering ethics , medicine , ethics committee , public relations , medical education , law , public administration , sociology , pathology , social science , engineering , psychiatry , physics , acoustics
Research ethics have become universal in their principles through international agreements. The standardization of regulations facilitates the internationalization of research concerning drugs. However, in so-called observational studies (i.e. from data collected retrospectively or prospectively, obtained without any additional therapy or monitoring procedure) the modalities used for applying the main principles vary from one country to another. This situation may entail problems for the conduct of multi-centric international studies, as well as for the publication of results if the authors and editors come from countries governed by different regulations. In particular, several French observational studies were rejected or retracted by US peer-reviewed journals, because their protocols have not been submitted to an Institutional Review Board/Independent Ethics Committee (IRB/IEC).
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