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.
F2F Meeting in Rome: Finalising the guidelines
The i-CONSENT Consortium met in Rome to give the final touches to the project's guidelines Consortium representatives sat the past November 4-6 around the table to give the final push the project's product. The i-CONSENT guidelines, with an innovative format, are...
i-CONSENT at the 25th Congress of Spanish Association of Bioethics
i-CONSENT participated the past October 25-26th in the 25th National Congress of the Spanish Association of Bioethics and Medical Ethics (AEBI ) held in Valencia. Topics such as human dignity, the ethics of the end of life, the ethics in assisted reproduction were...
i-CONSENT with Health Literacy Month 2019
6 reasons to participate in clinical trials October is #HealthLiteracyMonth and #iCONSENT is joining the celebration! For this purpose we explored 6 reasons why someone should participate in a #clinicaltrial. Before a treatment is commercialized it must undergo a...
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#DesignThinking | We are in Elche today holding a Design Thinking session with pregnant women and midwives, working on the inclusion of #gender perspective in our guidelines. Very interesting points where raised!
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