In September 2025, IFPMA organized a networking reception in New York on the margins of the UN General Assembly and the UN HLM on NCDs.
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From September to November 2025, the Africa Regulatory Conference presents a four-part webinar series on strengthening the clinical trial ecosystem in Africa. Building upon the WHO Global Action Plan for Clinical Trial Ecosystem Strengthening, the series convenes patients, communities, regulators, researchers, ethics bodies, civil society, and industry leaders to explore four core action areas where multi-stakeholder collaboration can drive progress for a more inclusive, innovative, and efficient clinical research environment.
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IFPMA is involved in several session at DIA Global, leveraging industry expertise on topics ranging from regulatory reliance, leveraging global standards to strengthen the drug supply chain, PQKMS and the evolving regulatory landscape in Africa.
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On the sidelines of WHA78 in May 2025, IFPMA organized an event focused on how health – a key driver for economic prosperity and national security – can remain a strategic priority through collaborative action and political leadership.
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IFPMA and member experts are attending DIA Europe 2025 and contributing to several sessions, leveraging industry expertise on regulatory agility, convergence, harmonization, and sustainable approaches to product design and post-approval changes. We are also demonstrating how adaptable regulatory systems can accelerate access to breakthrough innovations while ensuring supply chain resilience and continuity.
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Join us on 3-6 December 2024 for the next edition of the Asia Regulatory Conference, where we will explore the transformative power of regulatory collaboration across the region.
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In September 2024, IFPMA organized a networking reception in New York alongside the Summit of the Future, uniting global health leaders to build common ground on our approach to solving the biggest global health challenges.
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IFPMA hosted a webinar on the WHO facilitated regulatory pathways with speakers from the WHO Regulation and Prequalification Department, the European Medicines Agency and Swissmedic.
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