New project product: Clinical trials for vaccines by iCONSENT
The video describes the development of clinical vaccine trials and explains all you need to know before choosing to participate in one The video, elaborated by project partner GSK, explains vaccines’ lifecycle from its production in the laboratory to its...
i-CONSENT validation kicks-off in Spain
The team will evaluate the information materials created following the project guidelines The project validation starts today in Spain and will be followed by a validation in UK and Romania. This validation allows to present the materials elaborated following the...
Next steps for i-CONSENT
From WP2 and WP3 to the elaboration of the guidelines With approximately one year of project left, i-CONSENT is starting to translate the findings into a set of guidelines to improve Informed Consent. The conclusions of i-CONSENT WP1 (Work package 1, A...
Workshop: A step closer to improving Informed Consent
i-CONSENT presents the draft guidelines to main stakeholders in Brussels i-CONSENT has reached the second stage of the project. The draft guidelines for improving the Informed Consent Process are now finished and next step is its revision. The recommendations...
i-CONSENT presents first results in Rome
“Ethical and Legal Issues concerning Informed Consent”, seminar in Rome LUMSA team presented last Monday first i-CONSENT results within the seminar “Ethical and Legal Issues concerning Informed Consent” held in Rome. The...
📝El proyecto europeo i-CONSENT presenta sus guías para mejorar los procesos de consentimiento informado en estudios clínicos
📌Consulta la guía: https://i-consentproject.eu/wp-content/uploads/2021/03/Guidelines-for-tailoring-the-informed-consent-process-in-clinical-studies-2.pdf
🔗Más información: http://fisabio.san.gva.es/web/fisabio/noticia/-/asset_publisher/1vZL/content/iconsent-publicacion-guia
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