If you are thinking about entering the Brazilian market for the first time, understanding ANVISA’s regulatory requirements can be overwhelming. Information about medical device regulations on the ANVISA website can be confusing and does not tell the full story about how the registration process really works, or what is required of you as a manufacturer.
Free information packet makes it easier to understand the process in Brazil
To help medical device manufacturers who want to export medical devices to Brazil, we assembled a packet that includes the basic information you need before deciding to enter the Brazilian market. It outlines the registration requirements and ongoing obligations to maintain compliance.
Here is what we will send you
If you set aside just one hour to read/watch these items, we guarantee you will have a MUCH better understanding of how ANVISA’s regulatory process works.
