Ministero della Salute
Italian VersionAGENAS, in collaboration with the Control Room of Medical Device (Cabina di Regia), is in the process of developing a new Healthcare Technologies submission form. The goal is to enhance the usability and effectiveness of the phases in the medical device governance process outlined in the National Program HTA Medical Devices 2023-2025.
One of the responsibilities of the Control Room of Medical Device is to validate the methodological guidelines that will be applied for the production of HTA reports under the National HTA Program (PNHTA).
For technical reasons, the page of the web-site dedicated to reporting has been discontinued.
In this transitional phase, pending the validation of the updated version of the reporting form by the Cabina di Regia, in order to ensure the continuity of reporting.is necessary to write to hta@agenas.it in order to receive the dedicated form by e-mail.