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What You Can Learn from 7 Theme Fusion Success Stories
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Critical Role of Stakeholder Collaboration in Personalized Medicine for Rare Diseases
A significant contribution to the European Joint Programme on Rare Diseases (EJP RD) “Innovative Therapies and Personalized Medicine for Rare Disease” Massive Open [...]
Legal Expert Sheds Light on European Framework for Rare Disease Treatments
Dr. Éloïse Gennet, junior professor in European health law at Aix Marseille University, CNRS, DICE, CERIC, Aix-en-Provence, France, has contributed valuable [...]
Biobanking Expert Highlights Critical Role of Quality Biosamples in EJP RD MOOC
Prof. Angelo Paradiso, a leading figure in biobanking and former Scientific Director of Istituto Tumori, National Cancer Research Center in Bari, [...]
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 [...]
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 [...]
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 [...]
CVBF’s New Video Offers Insights into Multinational Rare Disease Clinical Trials
We are proud to share with you the newly released informative video detailing the challenges and strategies involved in conducting the DEEP- 2 clinical trial [...]
CVBF at the ERAMET Kick-Off Meeting
Namur, Belgium - CVBF participated in the kick-off meeting of the ERAMET project on March 4-5 in Namur that was organized by the University of [...]
29 February 2024, Rare Disease Day
29 February is Rare Disease Day, falling on the rarest date of the calendar. This is an opportunity to raise awareness that over 300 million [...]
CVBF’s Scientific Director to Speak at Rare Disease & Orphan Drugs Congress
Giovanni Migliaccio, Scientific Director of CVBF and member of the Board of Directors of the European Paediatric Translational Research Infrastructure (EPTRI), will be speaking at [...]
CVBF’s Head of Project Development, Arianna Bertolani, to Attend World EPA Congress 2024
Our Head of Project Development, Arianna Bertolani, as a member of the TEDDY Network Board of Directors, will be attending the World Healthcare Evidence Pricing [...]
Newsletter, February 2024
Newsletter, February 2024 Since 12 February 2024 we welcome you in our new offices in Pavia In a strategic move aimed at optimizing [...]