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.
i-CONSENT COVID-19 glossary of terms
i-CONSENT Project brings science and health closer to society by improving the communication between citizens and professionals. Initially, the Project was designed to make informed consent in clinical research more comprehensible to the participant. However, COVID-19...
Stimulating experts’ views on the challenges of digitalisation and policy developments in clinical research
This virtual workshop organised by i-CONSENT partner AND-CG offered the opportunity to explore different dimensions of informed consent-related practices Around 15 experts gathered yesterday morning for the i-CONSENT webinar "Rethinking informed consent: Emerging...
i-CONSENT organises a multi-stakeholder workshop to discuss ICT in informed consent
The workshop will take place online on the 26th of March The main goal is stimulating dialogue around the challenges presented for consent-related practices in the context of clinical research. The workshop will explore these challenges under the lens of technological...
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Article | #iCONSENT presents its #COVID19 glossary of terms. Discover the meanings of those big concepts that are currently all around our newspapers, social media or daily conversations and we might have troubles understanding.
🗯️#H2020 #Healthliteracy
🔗https://i-consentproject.eu/i-consent-covid-19-glossary-of-terms/