Aspectos destacados y características

What is happening at Latin America Annual Meeting

Gain exclusive insights into current and future trends in regulatory, clinical, and pharmacovigilance (PV) across Latin America
Hear directly from regional and global experts, including regulators, industry leaders, and key stakeholders shaping the future of drug development
Engage with high-impact sessions, plenary and concurrent tracks covering pressing topics in regulatory affairs, clinical operations, safety and PV
Access cross-functional discussions that highlight the interconnected nature of regulatory, clinical, and safety strategies
Explore region-specific challenges and opportunities, with solutions tailored for Latin America’s unique regulatory and public health environments
Expand your professional network with influential voices across industry, government, and academia
Take home actionable knowledge and best practices to strengthen compliance, streamline development, and improve healthcare outcomes
Participate in intimate, neutral forums that encourage collaboration and honest dialogue
Be part of the conversation shaping drug development policy and practice in Latin America and beyond

Track Alignment for 2026!

Regulatory/Clinical Track:

The regulatory/clinical track provides a dynamic platform to explore the evolving regulatory landscape and clinical research practices across Latin America. Participants will engage with case studies, best practices and emerging trends in life science R&D, with a special focus on integrating medical devices into regulatory and clinical frameworks. This track highlights innovative approaches to compliance, multi-regional cooperation, and practical strategies for the successful development and management of both pharmaceutical products and medical devices.

Safety and Pharmacovigilance Track:

Dive into the latest advancements in clinical safety and pharmacovigilance for pharmaceutical products and medical devices within the dynamic landscape of Latin America. Our safety and pharmacovigilance track offers attendees a deep dive into essential topics, including best practices, case studies, and regulatory compliance strategies, ensuring a comprehensive understanding of this critical aspect of the life sciences industry.

DIA Reliance Workshop

September 9, 2026 – 8:00AM – 12:00PM CT | In-Person
*Reliance Workshop requires an additional registration fee. You do not need to be registered for the forum to attend*

Across Latin America, stakeholders involved in the regulation and development of pharmaceuticals and medicines continue to explore and implement reliance approaches as a way to strengthen regulatory decision-making, optimize limited resources, reduce duplication of effort, and facilitate timely access to quality, safe, and effective medicines. While many agencies have introduced reliance pathways or referenced the work of trusted authorities, the operationalization of reliance in practice remains uneven across the region. Differences in regulatory frameworks, access to assessment reports, internal capacity, and levels of stakeholder engagement often create challenges when applying reliance consistently. As a result, there is increasing interest among regulators, the pharmaceutical industry, and other healthcare stakeholders to better understand how reliance can be implemented in practical, transparent, and sustainable ways.

This workshop will provide a neutral and educational forum for regulators and industry representatives to exchange perspectives on the current reliance landscape in Latin America and explore practical approaches for implementation. Rather than focusing on theoretical concepts, the discussion will emphasize real-world experiences, operational challenges, and opportunities to strengthen collaboration. Participants will hear examples from established international reliance models, including stakeholder engagement platforms and collaborative initiatives, and will discuss how similar approaches could inform regional efforts.

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