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San Diego Convention Center

Jun 16, 2024 7:00 AM - Jun 20, 2024 3:00 PM

111 W Harbor Drive, , San Diego, CA 92101 , USA

DIA 2024 Global Annual Meeting

Join us at the premier life sciences conference, celebrating our 60th anniversary! Discover 180+ sessions on Cell and Gene Therapy, Decentralized Clinical Trials, AI, ICH, and more. Get ready to tackle challenges, improve skills, network, and drive change for healthcare at DIA2024.

WHO Town Hall: Safeguarding Public Health - WHO's Vision for Global Regulatory Excellence

Session Chair(s)

Samvel  Azatyan, MD, PHD

Samvel Azatyan, MD, PHD

Senior Adviser, Council For International Organizations of Medical Sciences (CIOMS), Switzerland

This session aims to delve into WHO's pivotal role in the evolving landscape of global regulatory excellence. The discussion will revolve around the transformative impact of WHO-listed Authorities on medical product regulation, emphasizing regulatory reliance as a holistic approach to enhance efficiency and accessibility. Additionally, the session will address the pressing issue of substandard/falsified medical products and their potential threats to global health.

Learning Objective : Describe the significance of WHO-listed Authorities in shaping the future of medical product regulation; Examine the concept of regulatory reliance as a key strategy to enhance access and efficiency in global regulatory practices; Discuss the critical role of regulatory excellence in safeguarding public health against the threats posed by substandard/falsified medical products.

Speaker(s)

Hiiti  Sillo, MSC, RPH

Elevating Regulatory Reliance: The Strategic Impact of WHO-Listed Authorities in Transforming Global Regulatory Landscapes

Unit Head, Regulation and Safety, Department of Regulation and Prequalification, World Health Organization (WHO), Switzerland

Rutendo  Kuwana, RPH

Securing Supply Chains: A Global Imperative

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

Emer  Cooke, MBA, MSC

EMA Update

Chair, ICMRA; Executive Director, European Medicines Agency, Netherlands

Janis  Bernat, MSC

Industry Update

Director, Scientific and Regulatory Affairs, IFPMA, Switzerland

Marion  Laumonier, MSC

Moderator for Panel Discussion and Q&A

Technical Officer, Regulatory Convergence and Networks, World Health Organization (WHO), Switzerland

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