Next steps for i-CONSENT
From WP2 and WP3 to the elaboration of the guidelines With approximately one year of project left, i-CONSENT is starting to translate the findings into a set of guidelines to improve Informed Consent. The conclusions of i-CONSENT WP1 (Work package 1, A...
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...
i-CONSENT presents first results in Rome
“Ethical and Legal Issues concerning Informed Consent”, seminar in Rome LUMSA team presented last Monday first i-CONSENT results within the seminar “Ethical and Legal Issues concerning Informed Consent” held in Rome. The...
Press release Health literacy month
New EU project aims to improve guidelines for Informed Consent
The informed consent (IC) process allows the subject to voluntarily decide whether or not his/her participation in research. Therefore, autonomy of the patient in the decision of having a medical procedure or participating in clinical research is of major importance....
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