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.
Medical Device Regulations in Latin America covers topics such as:
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
Medical Device Regulations in Latin America brings together 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
Medical Device Regulations in Latin America might be held in London, United Kingdom in Sep 2020 (Not Final).