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.

i-CONSENT joins again European Researchers’ Night 2019

Engaging students through roll plays on the topic of informed consent The i-CONSENT team held interactive sessions for 16-18 years old students about informed consent at LUMSA University for the European Researchers’ Night 2019. More than 70 students had the...

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Our technical coordinator, @jaimefonsm, presented #iCONSENT before biobank experts from around Spain at the X #10CNbiobancos, highlighting the relevance of participants being the pillar within the IC processes. Interesting topics as participants portals or dynamic consent arose!

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i-CONSENT in Numbers

From 2017 to 2020

Partners

Million EU Funding

Countries

Years Duration

Multimedia

 i-CONSENT falls under the ‘Science with and for Society’ (SWAFS) programme, which means that finding ways of connecting science to society is one of its main goals. Well aware of this, i-CONSENT is committed to citizens’ health literacy not only as a solution to make science more attractive to them but also as a way of empowering them leading to a true autonomy and self-government when deciding to participate in health-related studies. This section will offer visitors and stakeholders information on the project, in particular, and  knowledge on clinical trials, research and ethics, in general.