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.
Inclusion of research participants from different cultural and religious backgrounds in clinical trials
Development of new strategies through “Design Thinking Exercise” methodology What are the most frequent doubts and concerns of research participants when they are offered the opportunity to enrol in a clinical study? How can we facilitate communication between...
read moreWOMEN 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...
read moreWorkshop: 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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