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.

New concept, new guidelines: conclusions after the meetings

i-CONSENT develops a route map for professionals involved in the design of informed consent process After three days of intense work, i-CONSENT can finally say that the process of elaboration of the guidelines is coming to an end. The project team flipped around the...

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F2F Meeting in Valencia: A step closer of our final product!

From today until Friday, Consortium members coming from UK, Italy and Spain will meet up again to discuss the draft version of the project's guidelines to improve informed consent. The meeting will take place in Valencia, at Fisabio's headquarters, and will focus on...

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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.