Understanding the Secondary Use of Clinical Trial Data: perspectives from patients, clinicians, industry, and regulators We are delighted to invite you to the II LET’s FACILITATE 2024 Webinar, an engaging exploration and roundtable discussion centered around the...
Fabrizio Cornia
An ethical-legal framework built on social alliance
At the 42nd National Congress of the Italian Society of Pharmacology, which was held in Sorrento, Italy, November 13-16, 2024, Veronica Rivi, from the Department of Biomedical, Metabolic and Neuroscience Sciences at UNIMORE and a member of FACILITATE, presented a...
Searching for reconciliation between law and ethics
At the 9th Conference of the European Association of Health Law, held at the University of Warsaw from September 18-20, Wenkai Li, a researcher from Vrije Universiteit Brussel, delivered an insightful presentation titled “Rethinking individual autonomy in the...
Clinical trial participants: no more study subject, but research partners
At the Clinical Research As A Care Option (CRAACO) Conference held in Philadelphia on September 16-18, 2024, Nadir Ammour, Global Lead, Clinical Innovation & External Partnerships, Sanofi and co-leader of the FACILITATE project, was the guest speaker in the panel...
Work in progress for patient-centricity
Download ENG PDF Download ITA PDF On June 20th, Marta García Manrique, R&D. Chief Patient Officer in Servier and representative in the FACILITATE consortium, presented the main features of the IHI project at the “Patient Centricity & Engagement Conference” in...
Together, for more equitable health
Download ENG PDF Download ITA PDF Once again IHI-FACILITATE project had a prominent space among the efforts devoted to responsible data sharing at the Drug Information Association (DIA) Global Annual Meeting hosted in San Diego from June 16-20, 2024. On Wednesday,...
Staunton C et al. Ethical framework for FACILITATE: a foundation for the return of clinical trial data to participants. Front Med 2024; 11:1408600
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Episode 3. What patients really want?
Veronica Popa, Digital Patient Engagement Manager at EURORDIS Rare Disease Europe, explores patients' views on the return and reuse of clinical trial data, explaining how it impacts their lives and why it is a priority to respect their needs and wishes.
Episode 2. Why FACILITATE, why now?
Johanna MC Blom, deputy coordinator of FACILITATE, traces the path of the project by explaining its rationale, analysing the context in which it was born, anticipating the concepts of ethical and legal frameworks, and emphasizing the benefits to stakeholders and...
Episode 1. Welcome to FACILITATE world
Johanna MC Blom, Professor of Psychobiology Paediatric and Behavioural Neuroscience at the University of Modena and Reggio Emilia and deputy coordinator of FACILITATE, introduces the project and its profound impact in the transformative world of clinical trial data...
Watch the webinar – Maximizing the societal benefit and lasting impact of clinical trials
Friday, 19 April 20242:00 to 3:30 pm CET Increasing stakeholder engagement and empowering participants to FACILITATE the effective return of clinical trial data Join us in the vision of this insightful overview and roundtable discussion of the FACILITATE...
A mutual work for patients’ empowerment
The return of individual data to clinical trial participants as a means of patient empowerment was once again featured at the annual Patients as Partners in Clinical Research US Conference, which took place in Philadelphia, Pa, on March 20-22nd. The theme of this...