Mejorando las pautas 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 pautas para mejorar el proceso de Consentimiento Informado, incluyendo las poblaciones vulnerables y la perspectiva de género y haciendo servir las nuevas tecnologías.
El Proyecto

Project guidelines now available!

Mar 25, 2021

The i-CONSENT Project publishes its final product: "Guidelines for tailoring the informed consent process in clinical studies" Fragment of the guidelines. The i-CONSENT Guidelines are now ready and available for academia, clinical investigators, pharmaceutical...

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H2020 project aimed to improve #informedconsent by focusing on gender, age and vulnerable populations to promote patient autonomy and empowerment through TIC.

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AvatarUNESCOBIOCHAIR@unescobiochair·
22 Nov

#NewPublication | "Cross-Cultural and Religious Critiques of Informed Consent" edited by Joseph Tham, Alberto García Gómez, Mirko Daniel Garasic.
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#InformedConsent

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Las cifras de i-CONSENT

Desde 2017 a 2020

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 i-CONSENT falls under the ‘Science with and for Society’ (SWAFS) programme, which means that on of our main goals is unlocking science for use by the wider public. i-CONSENT is committed to improving citizens’ health literacy not only as a solution to make science more attractive to them but also as a way of empowering them. This section will offer visitors and stakeholders information on the project, in particular, and  knowledge on clinical trials, research and ethics, in general.