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).
Due to the decree from the Minister of Health that revised the composition of the Control Room, awaiting the appointments and the establishment of the new Steering Committee, the updated version of the Health Technology Reporting Form, along with the removal of the currently accessible dedicated page on the website https://htadm.agenas.it/, will be postponed from the previously indicated date of mid-February 2024.
The update to the health technologies submission form is essential to streamline the prioritization process, which will take place between the end of March and the beginning of April 2024. This aims to formulate the work plan for the assessment throughout 2024.