Engage in sharing best practices with leading experts in an intimate and neutral setting
Be part of a diverse range of sessions, including plenary and concurrent tracks, covering the most pressing topics in regulatory, clinical, safety, pharmacovigilance, and medical affairs
Gain valuable insights from leading experts and key stakeholders who are driving initiatives and policies in the region
Benefit from cross-track sessions that provide a holistic view of the interconnectedness of regulatory, clinical, safety, and medical affairs efforts
Focused discussions on the unique challenges and opportunities in Latin America and the Caribbean, offering tailored solutions and strategies
Build meaningful connections with peers, industry leaders, and policy makers to foster collaboration and drive innovation
Obtain actionable knowledge and best practices that you can implement within your organization to enhance healthcare outcomes and regulatory practices
Engage in sharing best practices with leading experts in an intimate and neutral setting
Complimentary Content Preview Webinar: Unlocking Opportunities in Latin America: Trends, Membership, and Annual Meeting Insights On-Demand
Join us for an insightful 75-minute webinar focused on the upcoming DIA Latin America Annual Meeting and the wealth of membership opportunities available for stakeholders in the region. Our esteemed panelists and track chairs will discuss emerging trends in LATAM, share their experiences as DIA members, and highlight the benefits of DIA membership. This session aims to foster engagement, collaboration, and knowledge-sharing among stakeholders in Latin America. Don't miss this opportunity to connect with experts, learn about innovative trends, and explore the value of DIA membership.
The regulatory/clinical track offers a platform for sharing information, case studies, and best practices specific to Latin America's regulatory environment, encompassing regulatory compliance, emerging trends, and innovative approaches in life sciences R&D. Furthermore, this track will delve into the intricacies of clinical research development and operations within the industry.
Explore the latest advancements and regulatory updates in clinical safety and pharmacovigilance for pharmaceutical products and medical devices within the dynamic landscape of Latin America. Our safety and pharmacovigilance track offer 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.
Track 3: Medical Affairs and Scientific Communications Track:
Dive into our Medical Affairs and Scientific Communications track, where you'll gain tangible insights into navigating this dynamic landscape. Elevate your role as a medical affairs and communication professional and stay ahead in today's rapidly evolving healthcare environment.