Brazil's medical device regulatory update

In recent years, ANVISA released numerous regulatory updates to make Brazil a more accessible medical device market. Currently, the medical device industry has more transparency about the requirements for selling in Brazil. Medical device companies can expect several new regulations in the coming years, including new registration requirements. In this free webinar, we will examine current medical device registration requirements in Brazil and the future regulatory changes for medical devices.


• Overview of recent regulatory changes and current ANVISA registration requirements for medical devices
• New INMETRO compliance rules and deadlines 
• COVID-19 registrations and status
• ANVISA review timelines and expedited registration routes
• Overview of future regulatory changes

This webinar was recorded on June 24, 2021.