Medical Device Regulations in Latin America

Medical Device Regulations in Latin America is a course dedicated to this seminar will provide an essential overview of the key areas of requirements for approvals for Medical Devices in Latin America. Countries to be c.

Topics

• Benefits of attending:
• This new event will provide an essential overview of the key areas of requirements for approvals for medical devices in Latin America.Focusing on the regulatory requirements and developments in individual countries, the course will include interactive discussion to allow you to exchange experiences with other colleagues.
• Learn the definition of Medical device and their classification
• Understand medical device regulations in LATAM countries
• Discuss recent developments in the region LATAM
• Gain knowledge of the registration procedures
• Opportunities to meet, network and share experience with other industry collegues

Who should Attend

Attendees from:

• Anyone involved in the regulation for medical devices in LATAM
• This Seminar will be of particular interest to:
• Anyone interested in an update on recent developments
• Those who are new to working with medical devices in the region