Beyond 20 years of regulation, activity will address the prospects for sanitary control of products, software and cybersecurity.

Registration is now open for participation in the Regulatory Dialogue on the “20 years of Medical Device Regulation at Anvisa - next steps”. The activity will be held next November 6, in Brasilia, from 9h to 15h. The number of participants will be limited to the capacity of the Agency's auditorium, which is 240 people.

The program of the event includes the discussion of topics such as advances and regulatory perspectives in the country, highlighting the challenges related to customized medical devices, software and product cybersecurity.

The initiative is the result of a partnership between Anvisa and the Brazilian Association of Medical, Dental, Hospital and Laboratory Articles and Equipment Industry (Abimo) and the Brazilian Association of High Technology Industry for Health Products (Abimed).

Partners are also the Brazilian Association of Importers and Distributors of Health Products (Abraidi), the Brazilian Chamber of Laboratory Diagnostics (CBDL) and the Brazilian Alliance of Innovative Health Industry (Abiis).

At the end of the event, the exhibition “20 years of Medical Device Regulation at Anvisa” will be inaugurated.