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Virtual

Oct 13, 2025 9:30 AM - Oct 15, 2025 4:00 PM

(W. Europe Standard Time)

Middle East & Africa Conference (MEA)

Dive into three impactful days of knowledge-sharing, innovation, and collaboration at the virtual MEA conference from 13–15 October.

SESSION 10: Making the ME(N)A region a Clinical Trials hub

Session Chair(s)

Angelika  Joos, MPharm

Angelika Joos, MPharm

Executive Director, Science & Regulatory Policy

MSD, Belgium

Marco  Rafael, PharmD, MBA, RPh

Marco Rafael, PharmD, MBA, RPh

Regulatory Policy Leader

Roche, Switzerland

Overview This Session will highlight global, regional and local efforts to enhance the Clinical Trials environment. WHO will share how regulatory ecosystem optimisation can be a driver for trial activity, followed by AVAREF exploring cross-country collaboration between regulators and ethics committees. Regulators from Saudi Arabia, Tunisia, Egypt, and the UAE will share national initiatives to strengthen the CTs infrastructure and streamline approvals. The session will close with insights on data quality, patient recruitment, and health literacy in line with ICH and ethical guidelines.

Speaker(s)

Marwa  Al Abbas

National Initiatives for Ecosystem Strengthening, Regulatory Approval Predictability, Collaboration with Ethics Review Boards, Capacity Building and Infrastructure Investment

Marwa Al Abbas

Saudi Food and Drug Authority (SFDA), Saudi Arabia

Senior Clinical Trial Expert

Rania  Ibrahim

National Initiatives for Ecosystem Strengthening, Regulatory Approval Predictability, Collaboration with Ethics Review Boards, Capacity Building and Infrastructure Investment

Rania Ibrahim

Egyptian Drug Authority (EDA), Egypt

General Manager of The General Administration of Clinical Trials

Shaikha  Almazrouei

National Initiatives for Ecosystem Strengthening, Regulatory Approval Predictability, Collaboration with Ethics Review Boards, Capacity Building and Infrastructure Investment

Shaikha Almazrouei

Emirates Drug Establishment (EDE), United Arab Emirates

Director of the Reference National Laboratory – Drug Department

Rhanda  Adechina Adehan

Strengthening Technical Collaboration between Regulators and Ethics Committees across countries under the AMA Framework

Rhanda Adechina Adehan

World Health Organization (WHO), Switzerland

Technical Officer - Consultant AVAREF Secretariat

Abdul  Rouf Palli Valapila, PhD

Panel Discussion with Q&A (with the additional participation of):

Abdul Rouf Palli Valapila, PhD

Hamad Medical Corporation (HMC), Qatar

Director of Operations for Clinical Trial Unit

Mariem  Kadri

Panel Discussion with Q&A (with the additional participation of):

Mariem Kadri

ANMPS (Agence Nationale Du Médicaments et des Produits de la santé), Tunisia

Pharmacist - Directorate of Pharmacy and Medicine

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