The use of Clinical Trials Information System becomes mandatory for new clinical trial applications in the EU
According to the European Medicines Agency (EMA), from 31 January 2023, all initial clinical trial applications in the European Union (EU) must [...]
Implementation in the Italian legal system of the European Regulation 536/2014 on clinical trials
The Italian Minister of Health has signed the four decrees on Ethics Committees, thus taking a decisive step towards the full implementation [...]
CVBF is about to start a project to speed up and facilitate the diagnosis of celiac disease
The consortium consisting of IRCCS Materno Infantile “Burlo Garofolo” (Project Leader), Azienda Ospedaliera Universitaria Federico II, Azienda ULSS2 Marca Trevigiana and Consorzio [...]
Survey: International Clinical Trials Registry Platform (ICTRP) search portal user experience
In order to improve the user experience of the International Clinical Trials Registry Platform (ICTRP) search portal, the World Health Organization (WHO) [...]
CVBF spotlight on scientific literature: “Why children have to wait years for new drugs”
This recent article is part of Nature Outlook: Children‘s health and focuses on the lack of medicines approved for paediatric use. According [...]
First gene therapy to treat haemophilia B
EMA has recommended granting a conditional marketing authorisation in the European Union (EU) for Hemgenix (etranacogene dezaparvovec), the the first gene therapy [...]