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Conrad Cairo Hotel

Nov 25, 2024 6:00 PM - Nov 27, 2024 6:00 PM

1191 Nile Corniche, Cairo, 11221, Egypt

Middle East and North Africa Conference (MENA)

This two-day conference is designed for the industry's regulatory professionals to explore the evolving pharmaceutical landscape in the MENA region and address its unique challenges, with all regional regulators present.

Session 8: Suppy Chain & Sample Management

Session Chair(s)

Joerg  Garbe, PhD, MSc

Joerg Garbe, PhD, MSc

Global Quality Manager & Policy Lead

F. Hoffmann-La Roche Ltd, Switzerland

Doaa  Rady

Doaa Rady

Lot Release administration manager

Egyptian Drug Authority (EDA), Egypt

This Session will explore the global trend of using a Reliance-based waiver for in-country testing. Regulators will share their practical experiences with risk-based surveillance testing to replace import/registration testing. The goal of this session is to support regulators in the MENA region in optimising their testing systems to avoid waste of resources and ensure no delay of drug supply to patients.

Speaker(s)

Joerg  Garbe, PhD, MSc

Introduction: Global Trends and Regional Perspective

Joerg Garbe, PhD, MSc

F. Hoffmann-La Roche Ltd, Switzerland

Global Quality Manager & Policy Lead

Rutendo  Kuwana, RPh

WHO - Reliance for Sample Testing

Rutendo Kuwana, RPh

World Health Organization (WHO), Switzerland

Team Lead, Incidents and Substandard/Falsified Medical Products

Rania  Elafifi

Regional Perspective on In-Country Testing

Rania Elafifi

Roche, Egypt

Regulatory Affairs Lead - Egypt

Doaa  Rady

Practical Implementation of Risk-Based Strategies and Optimized Testing Systems in Egypt

Doaa Rady

Egyptian Drug Authority (EDA), Egypt

Lot Release administration manager

Pavle  Zelic

Risk-based Surveillance Testing in Serbia and How it Complements Anti-Counterfeit Activities in Serbia

Pavle Zelic

Medicines and Medical Devices Agency of Serbia (ALIMS), Serbia

International Cooperation, European Integrations and Public Relations

Rana  Malkawi

Panel Discussion with QandA, with the additional participation of:

Rana Malkawi

Jordan Food and Drug Administration (JFDA), Jordan

Drug Directorate Director

Agnes  Chan

Panel Discussion with QandA, with the additional participation of:

Agnes Chan

Health Sciences Authority, Singapore, Singapore

Director, Therapeutic Products Branch

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