Informed consent for paediatric clinical trials in Europe

OBJECTIVE: Paediatric clinical trials are often conducted as multinational trials. Informed consent or assent is part of the ethics committee approval for clinical trials. The consent requirements vary between countries due to national laws and regulations, which are not harmonised in Europe. These...

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Detalles Bibliográficos
Autores principales: Lepola, Pirkko, Needham, Allison, Mendum, Jo, Sallabank, Peter, Neubauer, David, de Wildt, Saskia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2016
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5136704/
https://www.ncbi.nlm.nih.gov/pubmed/27226526
http://dx.doi.org/10.1136/archdischild-2015-310001

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5136704/
https://www.ncbi.nlm.nih.gov/pubmed/27226526
http://dx.doi.org/10.1136/archdischild-2015-310001

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