i-CONSENT Guidelines start an audit process
The first meeting will be with Prof. Carlos Maria Romeo Casabona, expert in law and bioethics With the product nearly ready, it is time to give the guidelines a final revision. Experts from different fields such as law, bioethics, TIC, gender will be invited to...
What do pregnant women have to say about clinical studies?
New Design Thinking session with pregnant women to incorporate their input to the project’s perspective Following our sessions with kids, i-CONSENT met a group of volunteer pregnant women the past November 12th. The idea was to capture their views on informed...
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...
i-CONSENT at the 25th Congress of Spanish Association of Bioethics
i-CONSENT participated the past October 25-26th in the 25th National Congress of the Spanish Association of Bioethics and Medical Ethics (AEBI ) held in Valencia. Topics such as human dignity, the ethics of the end of life, the ethics in assisted reproduction were...
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...i-CONSENTFollow
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