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.
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...
Biomedical research involving health data in the context pandemic: implications for informed consent
LUMSA University organised Monday, March 22st 2021 the last meeting of its series of encounters to discuss informed consent in pandemic situations. This one, focused on ethical and legal requirements for biomedical research involving health data in the context of...
i-CONSENT presents its guidelines to improve informed consent in clinical studies
The project celebrated its final event: Towards the future of informed consent in clinical research. Yesterday, the i-CONSENT team finally presented its guidelines to improve informed consent in clinical studies. After 4 years of intense work and study in the...
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@ICONSENTEU
#Guidelines | Along with an introduction of the new #InformedConsent perspective, the #iCONSENT guidelines provide practical tools and recommendations to implement tailored and more understandable #InformedConsent processes. Haven't reviewed them yet? 👇
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