Regulation of Medical Devices in the Middle East and Africa

Regulation of Medical Devices in the Middle East and Africa
Understand the national requirements that must be met for approval of a medical device in the Middle East and North Africa (MENA) region. Look ahead to the impact of the MDR on approvals for medical devices in the region.


Date: Available on demand. (Original presentation November 2019)

 

Learning objectives

  • Broad view of the national requirements for these markets
  • Product Classification Criteria
  • Submission planning and approval timelines
  • Labelling requirements
  • Regulatory challenges for approvals and maintenance of products on the market
  • Impact of the MDR

 

Target Audience

Anyone wanting to get medical devices approved in the MENA region
Anyone working in the regulation of medical devices who wishes to gain a broader understanding of global markets


Speakers

Lea Atallah
Lea Atallah
Quality & RA Manager (MENA)
Zimmer Biomet

CPD

This course offers 1 CPD hour for successful completion, to learn about why CPD is important visit the Lifelong Learning page.

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Prices

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Standard    £70 + VAT £95 + VAT 
 

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Terms and conditions

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When
25/11/2019 15:00 - 16:30
Where
At Your Desk Middle East ONLINE
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