Registration Procedure of Medical Devices in Mexico and Brazil

Brazil and Mexico represents the two largest markets for Medical Devices in South America. However, manufacturers seeking to gain access to these two markets face significant hurdles.

In this seminar, we discuss and inform about the registrations in Brazil, Mexico and other countries of Latin America.

You will get information about similarities and differences to CE certification. In addition, there are inputs on the role of intermediaries operating in Latin America as a manufacturer and how you can successfully market products to the Latin American market with a good registration strategy.

Content

  • Submission documents
  • Competent authorities and country representations
  • Authority audits & necessary quality management systems
  • Typical obstacles and case studies
Details
Type: 
Inhouse
Target audience: 
This seminar is aimed at specialists and executives of Medical Device manufacturers. Staff from the following departments will benefit from the event: Regulatory Affairs, Quality Management, Product Management, Marketing, Sales.
Language: 
German (English on request)
Requirements: 
Knowledge of European Medical Device guidelines and EN ISO 13485 is recommended but not necessary.
Fee: 
480 Euro + 19% MwSt. = 571,20 Euro
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