CVBF supports the Rare Disease Day 2018
Again this year CVBF is glad to support The Rare Disease Day 2018, that will take place on 28th February 2018, to [...]
ERN-LUNG builds a new infrastructure for patient data management
In October 2017, the European Reference Network for rare diseases of the respiratory system (ERN-LUNG) won the competition for a grant from [...]
ID-EPTRI a new research infrastructure that will facilitate the future development of better paediatric medicines
Roma, January 2018 - ID-EPTRI (European Paediatric Translational Research Infrastructure) is a project coordinated by Consorzio per Valutazioni Biologiche e Farmacologiche (CVBF-TEDDY) [...]
An innovative approach for the patient involvement in the paediatric clinical research: the role of YPAGs
Over the last years, a Europe-wide trend towards a patient-focused approach and the involvement of patients is developing and is influencing the [...]
ICH-GOOD CLINICAL PRACTICE (GCP) TRAINING COURSE
The e-learning “ICH-Good Clinical Practice (GCP) Training Course”, promoted by Consorzio per Valutazioni Biologiche e Farmacologiche in the framework of the GAPP [...]
The pilot study QuBo was presented at the 14th International Conference on Thalassaemia & Haemoglobinopathies and 16th TIF International Conference for Patients & Parents
From November 17th to 19th, 2017, the 14th International Conference on Thalassaemia & Haemoglobinopathies and the 16th TIF International Conference for Patients [...]