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Conrad Cairo Hotel

2024 年 11 月 25 日 6:00 下午 - 2024 年 11 月 27 日 6:00 下午

1191 Nile Corniche, Cairo, 11221, Egypt

Middle East and North Africa Conference (MENA)

Session 8: Suppy Chain & Sample Management

Session Chair(s)

Joerg  Garbe, PHD, MSC

Joerg Garbe, PHD, MSC

IFPMA In-Country Testing Taskforce Lead; 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

Joerg Garbe, PHD, MSC

IFPMA In-Country Testing Taskforce Lead; Global Quality Manager & Policy Lead, F. Hoffmann-La Roche Ltd, Switzerland

Introduction: Global Trends and Regional Perspective

Rutendo  Kuwana, RPH

Rutendo Kuwana, RPH

Team Lead, Incidents and Substandard/Falsified Medical Products, World Health Organization (WHO), Switzerland

WHO - Reliance for Sample Testing

Rania  Elafifi

Rania Elafifi

Regulatory Affairs Lead - Egypt, Roche, Egypt

Regional Perspective on In-Country Testing

Doaa  Rady

Doaa Rady

Lot Release administration manager, Egyptian Drug Authority (EDA), Egypt

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

Pavle  Zelic

Pavle Zelic

International Cooperation, European Integrations and Public Relations, Medicines and Medical Devices Agency of Serbia (ALIMS), Serbia

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

Rana  Malkawi

Rana Malkawi

Drug Directorate Director, Jordan Food and Drug Administration (JFDA), Jordan

Panel Discussion with QandA, with the additional participation of:

Agnes  Chan

Agnes Chan

Director, Therapeutic Products Branch, Health Sciences Authority, Singapore

Panel Discussion with QandA, with the additional participation of:

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