Pharmaceutical Regulatory Affairs in the Middle East and North Africa In-house Training

Course overview

The course will equip participants with practical understanding and essential insights into the latest regulatory requirements and developments specific to individual countries within the Middle East and North Africa. 

Additionally, this course will explore regional initiatives aligned with global trends, including Common Technical Documents (CTD), and electronic Common Technical Documents (eCTD) submissions, and regional harmonisation efforts. With a strong emphasis on real-world application, this seminar aims to provide valuable knowledge for navigating the evolving regulatory landscape in one of the world's most dynamic pharmaceutical markets.

This course is part of our Regulatory Affairs Training course collection, which features updates on the latest regulations to registration procedures and strategies.

Benefits of attending

• Gain an overview of the regulatory environment in the Middle East and North Africa
• Understand the economic and cultural background to the markets
• Obtain insights regarding procedures for company and product registration
• Receive information about Dossier format in each country (CTD, eCTD or other)
• Examine harmonisation and recent developments in the region

Who should attend

This seminar will be of particular interest to:

• Personnel involved in pharmaceutical regulatory affairs in the Middle East and North Africa
• Anyone new to the region e.g. Regulatory Affairs, Pharmacovigilance, Market Access and Business Development leads
• All those interested in an update on recent developments