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.

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...

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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!
🗯️ #iCONSENT #H2020 #ResearchEU

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i-CONSENT in Numbers

From 2017 to 2020


Million EU Funding


Years Duration


 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.