Reporting Adverse Events of Medical Devices via e-Notivisa
ANVISA has announced an important update that will allow citizens to report adverse events related to medical devices directly through the e-Notivisa system. This new functionality is a step forward in the monitoring and control of the safety of health products, allowing a quick and effective response to potential problems. Reporting adverse events is essential to ensure that medical devices in use are continuously monitored, providing greater protection to public health.
This system increases society's participation in the surveillance process, allowing health professionals and users to contribute to the early identification of potential risks. Rapid action based on these reports helps in the implementation of corrective and preventive measures, ensuring that medical devices are always in compliance with the highest safety standards.
Our team is always available to help manufacturers and importers ensure that their products meet the market requirements of Anvisa and the certification requirements of Inmetro - National Institute of Metrology, Quality and Technology. Contact us.
Read more about e-Notivisa at https://lnkd.in/dbvU9KyM.
