Mar 25, 2021 | Sin categorizar, Press Release
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, pharmaceutical...
Dic 1, 2020 | Sin categorizar, Press Release
The FISABIO team sat together with experts in the field and discussed the guidelines’ content using the RAND/UCLA methodology In addition to the validation of the materials elaborated following the i-CONSENT guidelines, it has deemed necessary to...
Oct 14, 2020 | Sin categorizar, Press Release
The video describes the development of clinical vaccine trials and explains all you need to know before choosing to participate in one The video, elaborated by project partner GSK, explains vaccines’ lifecycle from its production in the laboratory to its...
Sep 15, 2020 | Sin categorizar, Press Release
The team will evaluate the information materials created following the project guidelines The project validation starts today in Spain and will be followed by a validation in UK and Romania. This validation allows to present the materials elaborated following the...
Jun 3, 2019 | Sin categorizar, Press Release
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...
Ene 30, 2019 | Sin categorizar, Press Release
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...
