Would you like to understand how to access the Medical Device market in Mexico, Brazil and Colombia?
Join us for this specialized webinar, where you will gain a clear and up-to-date overview of the regulatory requirements for Medical Device Registration in Mexico, Brazil, and Colombia, important medical technology markets in Latin America. Guidance will be provided concerning the medical device registration process with COFEPRIS, ANVISA, and INVIMA. With a direct focus on foreign manufacturers, we will explore the key aspects of the current regulatory framework of the three countries.
In this webinar, you will learn:
• How the registration and/or notification process works in Mexico, Brazil, and Colombia for Medical Devices.
• Key requirements for foreign manufacturers.
• Estimated timelines, required documentation, and the roles of legal representatives.
• Upcoming regulatory changes to consider in 2025.
Regulatory Business Development
ClarkeModet Spain
Regulatory Business Development
ClarkeModet Brasil
Country Managing Director
ClarkeModet Colombia
