Anvisa Returns to Publishing Medical Device Price Monitoring Data
Anvisa (the National Health Surveillance Agency) has announced the resumption of the publication of medical device price monitoring data in its Business Intelligence (BI) panels. The activity, which had been temporarily suspended, is now back, with improvements to the process and guarantees of greater efficiency and precision.
European Commission Launches Public Consultation on Medical Devices and In Vitro Diagnostics Regulations
The European Commission has launched a public consultation on medical device regulations. Participate by March 21, 2025, and contribute to their evaluation.
FDA issues preliminary guidance for medical devices with Artificial Intelligence
First Guidance to Provide Comprehensive Recommendations for Artificial Intelligence in Medical Devices for Developers
FDA issues preliminary guidance for medical devices with Artificial Intelligence
First Guidance to Provide Comprehensive Recommendations for Artificial Intelligence in Medical Devices for Developers