Improving the guidelines for Informed Consent

i-CONSENT, funded by the European Union H2020 programme, aims to improve the information that patients receive from clinical studies. Within the project, a series of guidelines to improve Informed Consent process will be created, including vulnerable populations, under a gender perspective and relying on ICT tools.

Project guidelines now available!

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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Publicación | ¿Cuáles son las claves para mejorar los procesos de #consentimientoinformado en estudios clínicos? 🥼

📚Este artículo recoge la experiencia y recomendaciones de nuestro proyecto @ICONSENTEU:
https://pubmed.ncbi.nlm.nih.gov/35894807/

📑Guías completas aquí: https://zenodo.org/record/4563938#.YuJ1oC0rx0s

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i-CONSENT in Numbers

From 2017 to 2021

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Million EU Funding

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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.