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Pharmaceutical Regulatory Affairs in the Middle East


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Who should attend?

This seminar will be of particular interest to: Anyone involved in pharmaceutical regulatory affairs in the Middle East Anyone new to the region Anyone interested in an update of recent developments

Details

COURSE OVERVIEW

Countries to be covered include: Bahrain, Egypt, Iran, Iraq, Jordan, Kuwait, Lebanon, Libya, Oman, Palestine, Qatar, Saudi Arabia, Sudan Syria, UAE, Yemen

BENEFITS OF ATTENDING THIS MEETING

  • Gain an Overview of the Regulatory Environment in the Middle East
  • Understand the Economic and Cultural Background to the Markets
  • Clarify Procedures for Company and Product Registration
  • Discuss Harmonisation and Recent Developments in the Region
  • Centralised Registration in the Gulf (GCC-DR)
  • Middle East Regulatory Conference (MERC)
  • MERC Follow-up Activities
  • Industry Regulatory Groups and Activities

WHY YOU SHOULD ATTEND

This seminar will provide you with an essential overview of the key areas of regulatory affairs in the Middle East. This two day course will focus on practical aspects to assist with regulatory affairs in the region. The course will include interactive discussion sessions to allow you to exchange experiences with other delegates.

WHO SHOULD ATTEND

This seminar will be of particular interest to:

  • Anyone involved in pharmaceutical regulatory affairs in the Middle East
  • Anyone new to the region
  • Anyone interested in an update of recent developments

Prices

TBC

Contact

Leigh White
info@management-forum.co.uk

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