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 vulnerables y bajo una perspectiva de género, ayudándose de las nuevas tecnologías.
The i-CONSENT’s top 5 must-read news stories of 2019
Which of our news articles have catch the eyes of physicians, industry, and medical students more this year 2019? Find a compilation of our most popular posts! 1. i-CONSENT celebrates Women and Girl in Science Internacional Day The winner is this post celebrating the...
i-CONSENT Guidelines start an audit process
The first meeting will be with Prof. Carlos Maria Romeo Casabona, expert in law and bioethics With the product nearly ready, it is time to give the guidelines a final revision. Experts from different fields such as law, bioethics, TIC, gender will be invited to...
What do pregnant women have to say about clinical studies?
New Design Thinking session with pregnant women to incorporate their input to the project's perspective Following our sessions with kids, i-CONSENT met a group of volunteer pregnant women the past November 12th. The idea was to capture their views on informed consent...
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Event | Some pictures of our intervention today during the #NewHorrizon workshop. Our colleague @DafinadO presented our project and possible collaboration opportunities with the Social Lab 15!
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