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.
Call for Topics Open!
Submission Deadline: January 9, 2026
We are seeking topics submissions from professionals like yourself, aiming to gain a better understanding of your professional needs and the type of content we should focus on for the DIA Latin America Annual Meeting agenda.
¿Tiene una cuenta?