The i-CONSENT Project publishes its final product: “Guidelines for tailoring the informed consent process in clinical studies” Fragment of the guidelines. The i-CONSENT Guidelines are now ready and available for academia, clinical investigators,...
LUMSA University organised Monday, March 22st 2021 the last meeting of its series of encounters to discuss informed consent in pandemic situations. This one, focused on ethical and legal requirements for biomedical research involving health data in the context of...
The project celebrated its final event: Towards the future of informed consent in clinical research. Yesterday, the i-CONSENT team finally presented its guidelines to improve informed consent in clinical studies. After 4 years of intense work and study in the...
Our partner LUMSA University organised Monday, March 1st 2021 a meeting to further discuss the different emerging ethical problems and implications that COVID-19 has for informed consent. This time, the team invited Prof. M. Toraldo Di Francia to discuss the...
New project publication featured in BMC Medical Ethics journal Providing understandable information to patients is necessary to achieve the aims of the Informed Consent process. In recent decades, new, primarily digital technologies have been used to apply and test...
The i-CONSENT project is coming to an end. After 4 years of intense work and study in the field of clinical research and bioethics we are proud to inform you that the project guidelines are ready for publication. These guidelines are the result of profound...
📝El proyecto europeo i-CONSENT presenta sus guías para mejorar los procesos de consentimiento informado en estudios clínicos
📌Consulta la guía: https://i-consentproject.eu/wp-content/uploads/2021/03/Guidelines-for-tailoring-the-informed-consent-process-in-clinical-studies-2.pdf
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