fondazione per la ricerca farmacologica
gianni benzi onlus
Fondazione per la Ricerca Farmacologica Gianni Benzi Onlus is a Scientific Research Organisation, registered as a private, not-for-profit Foundation in 2007, with the aim to promote research in biological, medical and pharmaceutical areas in support of the development of innovative and safe medicines in Europe.
Discover more about us through this video.
HIGHLIGHTS
Delve into some of the most important activities now running at Fondazione Gianni Benzi
The new project ERAMET
The Foundation has recently started a new 4-year project, starting on January 1, 2024, funded under the Horizon Europe Framework Programme, titled ERAMET. Its kick-off meeting was held in Namur, Belgium, on March 5-6. The project aims to enhance decision-making and...
SAVE THE DATE: EJP RD Final Conference – Bari (Italy)
The EJP RD final conference will take place from 27 to 28 May 2024 in Bari, Italy and online. Registrations are open until 31 March 2024
Keep updated on all the initiatives and events of the Gianni Benzi Onlus Foundation dedicated to the comparison of research and training topics.
INTERNATIONAL THALASSAEMIA DAY – GIANNI BENZI FOUNDATION FOR RESEARCH AND IMPROVING PATIENTS’ LIVES
On the occasion of International Thalassaemia Day, celebrated every year on May 8th, Fondazione Gianni Benzi reaffirms its commitment to the fight against this genetic blood disease. Thalassaemia represents a major public health challenge, affecting thousands of...
New article published on data sharing for paediatric clinical research
On 20 April, the new article “Mapping of Data-Sharing Repositories for Paediatric Clinical Research-A Rapid Review” was published in Data, a peer reviewed MDPI’s open access journal. The paper discusses the re-use of individual paediatric patient data from clinical...
Health Data Ethics & Regulatory Frameworks in Rare Disease Research: a free online course starting from May 6th
A new Massive Open Online Course (MOOC) on Health Data Ethics & Regulatory Frameworks in Rare Disease Research has been launched today! Developed as part of the European Joint Programme on Rare Diseases, in collaboration with the Rare Diseases Foundation, this...
New article published in the journal Frontiers in Medicine
The article “The creation of an adaptable informed consent form for research purposes to overcome national and institutional bottlenecks in ethics review: experience from rare disease registries” has been published in the journal Frontiers in Medicine on April 17,...