Mejorando las directrices para el consentimiento informado
i-CONSENT, financiado por el programa H2020 de la Unión Europea, tiene como objetivo mejorar la información que los pacientes reciben de los estudios clínicos. En el marco del proyecto, se elaborarán una serie de recomendaciones para mejorar el proceso de Consentimiento Informado, incluyendo a la población vulnerable y bajo una perspectiva de género, ayudándose de las nuevas tecnologías.
i-CONSENT validation kicks-off in Spain
The team will evaluate the information materials created following the project guidelines The project validation starts today in Spain and will be followed by a validation in UK and Romania. This validation allows to present the materials elaborated following the...
«Might the digitalisation of clinical research lead to questioning the effectiveness of IC as a protection of participant autonomy?»
i-CONSENT publishes a report with the conclusions extracted from its virtual workshop “Rethinking informed consent: emerging challenges in the digital era” The document provides an overview of the online workshop organized by AND-CG and held on 26 March 2020. The...
How to tailor health information to our audience
Strategies and tools to know societies’ concerns and address them in our health messaging, especially in the current COVID-19 emergency Adapting information to the audience is crucial to meet their needs and values. These are unique and influenced by multiple factors...
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