Caterina Di Costanzo
Assegnista di ricerca, Università degli studi di Firenze
Sommario: 1. Introduction. – 2. State of the art in the relevant sectors for the purposes of the investigation. – 2.1. The framework of telemedicine at the European level. – 2.2. Informed consent in clinical trials. – 3. The interconnection of sectors at the time of covid-19. – 3.1. The supranational guidelines in the health emergency. – 3.2. The national guidelines in the health emergency. – 3.3. Indications from non-European States domestic farmeworks. – 4. Concluding remarks.
Clinical trials at the times of covid-19 in a public law perspective: telemedicine and changes to informed consent