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.
Towards the future of informed consent in clinical research
The i-CONSENT project is coming to an end. After 4 years of intense work and study in the field of clinical research and bioethics we are proud to inform you that the project guidelines are ready for publication. These guidelines are the result of profound...
Research protocols and Covid-19: elements for adequate patient information
Following the first session in November, project partner LUMSA University, deemed necessary, given the high level conversation and fruitful discussions, the organization of an additional meeting with expert Dr. Antonio Addis. In this second meeting, Dr. Addis started...
Improving Informed Consent for Novel Vaccine Research in Pediatrics
New project article reflecting on informed consent for vaccine research in pediatric population published in Frontiers in Pediatrics Journal Project partners OPBG, LUMSA and AND CG have published a new article today. The paper is called "Improving Informed Consent for...
Visita nuestro Twitter y disfruta de nuestro contenido actualizado!
@ICONSENTEU
Mark in your calendar March 16th, 2021 4-6pm virtual event to present the the project guidelines @ICONSENTEU https://bit.ly/37u2EaT https://twitter.com/ICONSENTEU/status/1361646513303085057
Event | The #iCONSENT guidelines to improve #informedconsent processes are ready for publication.
Join us in "Towards the future of informed consent in clinical research", a virtual meeting to present them on March 16th 2021 at 16:00h
Register here: http://conferenciasweb.es/i-consent/