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What You Can Learn from 7 Theme Fusion Success Stories
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Big Data and Machine Learning in Personalized Medicine: Insights from the EJP RD’s MOOC
The landscape of healthcare is rapidly evolving, with big data and machine learning at the forefront of this transformation. In the EJP [...]
Donato Bonifazi, CVBF’s CEO to Represent TEDDY, the European Network of Excellence for Paediatric Research, in the ACT EU Multi-Stakeholder Platform Annual Meeting
We are pleased to announce that our CEO, Donato Bonifazi, a permanent member of the Advisory Group of the ACT EU Multistakeholder [...]
Giovanni Migliaccio: Advancing Personalised Medicine for Rare Diseases
In the realm of rare disease research and education, collaboration and knowledge sharing are paramount. Giovanni Migliaccio, the CVBF’s Scientific Director and [...]
Our CEO to Present at Prestigious Global CardioVascular Clinical Trialists Workshop
We are proud to announce that Donato Bonifazi, CVBF’s CEO and Member of the Board of Directors of the Teddy [...]
Innovative Therapies and Personalized Medicine for Rare Diseases: MOOC in Full Swing
As we are in full swing of the facilitation window in September, we're excited to share an update on the [...]
Newsletter, June 2024
Dear Reader, Imagine a world where every child, regardless of their condition, has access to safe, effective, and child-friendly [...]
RACE Act accelerates Paediatric Oncology Drug Testing, FDA reports
The U.S. Food and Drug Administration (FDA) has reported a significant increase in the number of planned studies to [...]
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CVBF Attends EJP RD Final Conference in Bari
CVBF was among the participants at the European Joint Programme on Rare Diseases (EJP RD) Final Conference, held on 27-28 May 2024 in Bari, Italy. [...]
CVBF’s CEO represents TEDDY in EnprEMA as a member of the Coordinating Group
Donato Bonifazi, CEO of CVBF and a member of the Board of Directors of the Teddy European Network of Excellence for Paediatric Clinical Research, [...]
Virtual Cohorts for Paediatric Rare Disease Research
CVBF embraces an innovative computational approach to advance research in paediatric rare diseases, involving the creation of virtual patient cohorts and the use of in [...]
OrphaDev4Kids Project Commences with Kick-Off in Bari
The OrphaDev4Kids project, focused on advancing medical devices development for rare diseases in children, will officially launch with a kick-off meeting on 19 July 2024 [...]
EPTRI’s 2024 Scientific Meeting
The European Paediatric Translational Research Infrastructure (EPTRI) has exciting news to share about its upcoming Scientific Meeting and legal incorporation as an international non-profit [...]
iCAN 2024 Advocacy and Research Summit
Mark your calendars! The 2024 iCAN Advocacy and Research Summit is scheduled to take place from 15-19 July in Bari, Italy. This event brings together [...]