Middle East And North Africa Pharmaceutical Regulatory Affairs Course: CTD, ECTD Submissions, And Regional Harmonisation Efforts (ONLINE EVENT: June 2Nd - June 4Th, 2026)

(MENAFN- GlobeNewsWire - Nasdaq) Key market opportunities lie in understanding regional regulatory developments in the MENA region, harmonizing with global trends like CTD and eCTD submissions, and navigating the dynamic pharmaceutical landscape through practical application of new insights.

Dublin, April 14, 2026 (GLOBE NEWSWIRE) -- The "Pharmaceutical Regulatory Affairs in the Middle East and North Africa (June 2nd - June 4th, 2026)" training has been added to ResearchAndMarkets's offering.

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 course aims to provide valuable knowledge for navigating the evolving regulatory landscape in one of the world's most dynamic pharmaceutical markets.

Who Should Attend:

• 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

Key Topics Covered:

Day 1

• Introduction to Regulatory Affairs in the Middle East and North Africa
• Economic overview of the Middle East and North Africa
• Saudi Arabia
• Harmonisation and recent developments
• Bahrain
• Qatar
• Oman
• Kuwait
• Real case examples

Day 2

• UAE
• Yemen
• Sudan
• Egypt
• Libya
• Lebanon
• Jordan
• Syria
• Iraq

Day 3

• Algeria
• Morocco
• Tunisia
• Palestine
• Israel
• Iran
• Local trade associations
• MENA Regulatory Conference
• Case studies for practical application

CPD Hours: 18
Speakers

Ilona Putz

Ilona Putz is the founder and General Manager of PULONA Emerging Markets based in the UAE since company is dedicated to creating and developing tailor-made business concepts including regulatory consultancy for international manufacturers in the healthcare sector across the Middle East.

Ilona has worked in the Pharmaceutical Industry since 1988 for companies like MSD, SmithKline Beecham, Karl Engelhard, HEXAL and Sandoz where she was the Regional Head, Middle East, for Sandoz International, Germany, responsible for all commercial and business development also consults for RegAff, Emergo and Dr. Regenold GmbH for the Middle spoke during the DIA Europe Meeting on "Clinical Trials in the Middle East" and at the Global Pharmaceutical Regulatory Affairs Summit 2021.

Heba Hashem

Heba has been working with Regulatory Affairs in the Middle East for more than 25 years. She has a Pharmaceutical and Business background being a graduate of the Faculty of Pharmacy (Cairo University), RAC certified in addition to an MBA at Maastricht School of Business. For the past 20 years Heba held the position of Middle East & Africa Regulatory and Quality Head at different Pharmaceutical and Medical Device companies; Gambro, Bayer and Novo Nordisk.

Heba is now the Middle East and Africa Associate Director at PPD where she is providing regulatory consulting services and training to Health Care companies.

For more information about this training visit

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