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This webinar will discuss the basics of product registration in Mexico, Brazil and Argentina such as Registration Timelines, documentation requirements and governmental processes.
Why Should You Attend:
While Brazil has long been pre-eminent in Medical Device regulation and registration, other countries in Latin America have followed suit, especially in Mexico and Argentina.
Mistakes in registration dossiers or noncompliance to the registration processes result in significant registration timeline delays or potential resubmission of product dossiers.
This webinar will lay a clear foundation for the firm’s education on registration in these three important Latin American countries.
All medical device companies wishing to do business in these countries will need to submit product dossiers for review prior to sale of products in those countries. This webinar will teach you what is required as well as governmental interactions and processes.
Areas Covered in the Webinar:
Who Will Benefit:
From Medical Device Companies
Physical CD-DVD of recorded session will be despatched after 72 hrs on completion of payment
With over 40 years of experience in the medical device industry, Mr. Riggi’s success spans the following industry sectors:
Mr. Riggi brings this extensive experience to the client in the areas of:
Whether on the manufacturing floor or in front of large conference audiences, Mr. Riggi's open and relaxed communication talents ensure maximum value for the client.