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.

WOMEN AND GIRLS IN SCIENCE INTERNATIONAL DAY

Science and gender equality are both vital for development, yet today full and equal access to research is a privilege of the few. This problem affects women and girls to a greater extent who have been traditionally pushed away from certain fields.  Women and girls...

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Workshop: A step closer to improving Informed Consent

i-CONSENT presents the draft guidelines to main stakeholders in Brussels i-CONSENT has reached the second stage of the project. The draft guidelines for improving the Informed Consent Process are now finished and next step is its revision. The recommendations...

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Prof. Barbara Prainsack, Kings College London, visited today #iCONSENT's @UniLUMSA team in Rome to discuss new #strategies for increasing participation of patients from diverse cultural and religious backgrounds in #clinicaltrials. Engaging discussion!
🔗https://t.co/3uZUTSAFGW

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i-CONSENT in Numbers

From 2017 to 2020

Partners

Million EU Funding

Countries

Years Duration

What is informed Consent?