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NH Buenos Aires City

Sep 29, 2025 1:00 PM - Oct 01, 2025 12:00 PM

Bolívar 160, C1066AAD Buenos Aires, Argentina

Latin America Annual Meeting

Take advantage of opportunities for networking and knowledge sharing with key stakeholders influencing the advancement and implementation of initiatives in Latin America.

Early Bird Rates in effect until

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Overview

Meeting: September 29 – October 1

DIA’s 2025 Latin America Annual Meeting offers unparalleled opportunities for networking and knowledge sharing with key stakeholders to advance and implement life sciences R&D initiatives in Latin America and the Caribbean. This year, session tracks on Regulatory/Clinical and Safety and Pharmacovigilance expand the scope of the meeting, with cross-track sessions facilitating discussions on key connection points across these areas to promote collaboration and synergy within organizations.

Join the conversation on multi-regional cooperation, global harmonization and reliance, lessons learned, and best practices. Don’t miss the chance to be part of this pivotal event, where innovation and cooperation come together to shape the future of healthcare in the region.

*The primary language is English, however simultaneous interpretation in Spanish and Portuguese will be available during this meeting.

While we develop our 2025 agenda, please take a moment to review the 2024 final agenda.

Participant Testimonials

DIA Latin America Annual Meeting offers unparalelled networking opportunities and knowledge sharing. It brings together outstanding scientists, impactful regulatory professionals and influential academic researchers to help advance discovery and innovation in regulatory science and policy in the LATAM region. - Viktoria Magyar, USC Alfred E. Mann School of Pharmacy and Pharmaceutical Sciences, United States

DIA offers a valuable opportunity to network with industry professionals, stay updated on the latest market trends, and gain insights into evolving regional regulations. - Jaime Cevallos, Risk Profile Technical, ARCSA, Ecuador

DIA LAAM 2024 was a great opportunity for networking and valuable insights! - Isabelle Campos, Pharmacovigilance Manager, GSK, Brazil

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Exhibits

Highlights & Features

Who should attend?

  • Professionals interested in:

    • Academia
    • Benefit-Risk Assessment and Communication
    • Clinical Research and Development
    • Clinical Operations
    • CROs/Vendors
    • Document Management/eSubmissions
    • Drug Regulation
    • Drug Safety/Pharmacovigilance
    • Field Medical
    • Global Submission/Project Management
    • Government Affairs
    • Manufacturing
    • Medical and Scientific Affairs
    • Medical Call Center Environment
    • Medical Communications
    • Medical Information
    • Medical Product Safety Assessment
    • Medical Science Liaisons
    • Medical Writing
    • Patient Engagement and Advocacy Groups
    • Pharmacoepidemiology
    • Policy and Intelligence
    • Post-Market Studies
    • Quality Assurance and Compliance
    • Real-World Evidence Generation
    • Regulatory Agencies
    • Regulatory Affairs, Operations, and Strategy
    • Research and Development
    • Risk Management, including Risk Evaluation and Mitigation Strategies (REMS)
    • Strategic Sourcing/Planning

Program Committee

  • Flavia  Firmino Ribeiro, PharmD
    Flavia Firmino Ribeiro, PharmD Global Regulatory Policy Lead Latin America
    Eli Lilly and Company, Brazil
  • Raphael Elmadjian Pareschi, PharmD, MBA
    Raphael Elmadjian Pareschi, PharmD, MBA Patient Safety Lead/ Head of Pharmacovigilance Brazil
    Roche, Brazil
  • Daniela  Bravo
    Daniela Bravo Regulatory Policy and Intelligence Manager
    AbbVie, Brazil
  • Arthur  Bueno, PharmD, MBA
    Arthur Bueno, PharmD, MBA Country Safety Head Back-Up
    Sanofi Brazil, Brazil
  • Martin  Cabrera Carchio
    Martin Cabrera Carchio International Relations Advisor
    ANMAT Ministry of Health, Argentina
  • Johnny  Karini, MD
    Johnny Karini, MD Head of Life Sciences & Health Care - US, LATAM
    Tata Consultancy Services, India
  • Yoon Jeon (Jamey)  Kim, MSc, RPh
    Yoon Jeon (Jamey) Kim, MSc, RPh Director, Cluster Pharmacovigilance Lead
    Merck & Co., Inc., Rahway, NJ, USA, Panama
  • Susan  Koepke, MBA
    Susan Koepke, MBA Head of Regulatory Affairs LATAM
    EMD Serono, Inc., United States
  • Lawrence  Liberti, PhD, RAC
    Lawrence Liberti, PhD, RAC Director, D.K. Kim International Center for Regulatory Science
    The Kim Center/ USC DRQS, United States
  • Mercedes Paloma Lopez, MA
    Mercedes Paloma Lopez, MA Regional Operations Manager, Latin America
    WCG Clinical, United States
  • Rosana M. Mastellaro, PharmD, RPh
    Rosana M. Mastellaro, PharmD, RPh Director, Technical Regulatory Affairs and Innovation
    Sindusfarma, Brazil
  • Ana  Pineda Zavaleta, MSc
    Ana Pineda Zavaleta, MSc International Regulatory Analyst, LAO, OGPS, OPLIA, OC
    FDA, United States
  • Diego Alexander Salas, LLM
    Diego Alexander Salas, LLM Regulatory Affairs Director
    Federación Latinoamericana de la Industria Farmacéutica, A.C., Mexico
  • Carolina  Sian
    Carolina Sian Regulatory Affairs Manager
    CAEME, Argentina
  • Gislaine Villarta Capeleti Dib, PharmD
    Gislaine Villarta Capeleti Dib, PharmD Patient Safety Manager
    PGA Farma, Brazil
  • Bianca  Zimon, LLM
    Bianca Zimon, LLM Health Regulation Specialist
    ANVISA, Brazil
  • Representative Invited
    Representative Invited Irish Dental Association, Ireland

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