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Medical Device Regulations in Latin America


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Who should attend?

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

Details

Course overview 

This new seminar 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.

Benefits of attending:

  • Understand medical device regulations in LATAM countries
  • Learn the definition of Medical device and their classification
  • Gain knowledge of the registration procedures
  • Discuss recent developments in the region LATAM
  • Opportunities to meet, network and share experience with other industry collegues

Prices

GBP 699.00 EUR 979.00 USD 1,090.00 + VAT @ 20.00% Book before 21 December 2018 to get an EBD GBP 599.00 EUR 839.00 USD 934.00

Contact

Leigh White
info@management-forum.co.uk

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