Regulatory Affairs in the Middle East and Africa

Regulatory Affairs in the Middle East and Africa
This webinar will provide an introduction to the regulatory environment and registration process in the Middle East and Africa.


When: On-demand - This is a recording of the live webinar which took place in May 2018.



Learning objectives 

  • Understand the pharmaceutical environment and business culture in the Middle East and Africa
  • Understand the regulatory environment/processes in the key countries in the region
  • Understand what the most important/critical requirements are in order to register pharmaceutical products in the Middle East and Africa
  • A better understanding of how regulatory lifecycle management works in the Middle East and Africa

Target audience  

This webinar is designed for regulatory professionals who are interested in markets in the Middle East and Africa - especially those who work on lifecycle management, CMC, labelling or product development Phase 3.


Hussein Sabtiy is the Director of Regulatory Affairs, NEMEA (Near East, Middle East and Africa) Region, at Takeda. He has over 13 years of regulatory experience within the EU and emerging markets. He holds a Masters in Pharmaceutical Science from The Danish Pharmaceutical University.    


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

How do I register?

Simply log in or create an account and register below. 


Type Member  Non-member 
Standard    £75 + VAT £95 + VAT 

Discounted Places

A limited number of discounted places are available at the rates below for those:

Please email for a discount code before making your booking.

Type Member  Non-member 
Discount  £35 + VAT*  £47.50 + VAT* 

* VAT, if applicable, is charged at a rate of 20%.

Terms and conditions

Please read the training terms and conditions before booking this webinar. By booking this webinar, you are agreeing to the terms and conditions.

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