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Administrative complexities for a European observational study despite directives harmonising requirements
Author(s) -
Gülmez Sinem Ezgi,
LignotMaleyran Séverine,
de Vries Corinne S.,
Sturkenboom Miriam,
Micon Sophie,
Hamoud Fatima,
Blin Patrick,
Moore Nicholas
Publication year - 2012
Publication title -
pharmacoepidemiology and drug safety
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.023
H-Index - 96
eISSN - 1099-1557
pISSN - 1053-8569
DOI - 10.1002/pds.3204
Subject(s) - observational study , multinational corporation , authorization , medicine , directive , population , expert opinion , family medicine , accounting , environmental health , business , finance , programming language , intensive care medicine , computer security , pathology , computer science
ABSTRACT Purpose For pharmacoepidemiological studies in Europe, accessing data should require only authorisation by the relevant data protections committees, as expected from the 1995 Data Protection Directive (95/46/EC). Our experience from a multinational observational study across seven European countries shows that this is certainly not the case. Methods The study was a multicentre, multinational, case‐population study in European liver transplant centres in seven countries, retrospectively evaluating a 3‐year period. Before data collection started, the procedures to obtain the necessary authorisations for the participating countries were defined. Remarks In France, a single opinion from a single data protection committee was enough to start the study. In Italy, Portugal, Greece and the UK, there was a national authority, but the hospitals requested the approval by their local committees/bodies irrespective of whether the authorisation of the national committee came after or before that of local ones. In Ireland, only one hospital participated, and the opinion of its ethics committee was sufficient. In the Netherlands, the opinion of the institutional review board of the local coordinating centre was necessary to obtain the opinions from the institutional review boards of the other hospitals. The information requested by the different committees and the time to obtain the approvals varied, even within the same country. Conclusion This degree of complexity and disharmony, and resulting cost, was observed in a simple retrospective study. Regulators will need to be aware that these time‐consuming, expensive and useless complexities must be factored in when estimating the time and cost of a study. Copyright © 2012 John Wiley & Sons, Ltd.