Improving the guidelines for Informed Consent
i-CONSENT, funded by the European Union H2020 programme, aims to improve the information that patients receive from clinical studies. Within the project, a series of guidelines to improve Informed Consent process will be created, including vulnerable populations, under a gender perspective and relying on ICT tools.
It is generally agreed that informed consent is a process whose effectiveness is a factor of a few core criteria. These criteria are typically held to include concepts such as disclosure, understanding, capacity, and voluntariness. Though guidelines differ somewhat in...read more
The VI ANCEI Congress was celebrated on May 30 and 31 in Tarragona For second year in a row, the i-CONSENT project participated in the ANCEI Congress in its VI edition, taking the first project results before the Spanish Research Ethic Committees. i-CONSENT...read more
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...read more