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Overview

Join global regulators, industry, and academia to engage in a series of strategic discussions on current regulatory landscape, globalization, and harmonization initiatives in Latin America.

DIA brings you a symposium with interactive dynamics, where you will be engaged in discussions with key stakeholders influencing the advancement and implementation of regulatory convergence initiatives in Latin America.

Join us to discuss multi-regional cooperation, global harmonization, and best practices related to Latin America’s regulatory landscape. Sessions will highlight regulatory approaches and good practices to ensure reliance in Latin American and strategic initiatives to improve collaboration and cooperation.

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Continuing Education

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Exhibits

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Who should attend?

Professionals involved in:

  • Drug Regulation
  • Clinical Research and Development
  • Medical and Scientific Affairs
  • Quality Assurance
  • Research and Development
  • Strategic Sourcing/Planning
  • Regulatory Affairs

Learning objectives

At the completion of this conference, the participant should be able to:
  • Identify the current regulatory landscape across Latin America including updates on harmonization and convergence efforts, and individual regional priorities from various National Regulatory Authorities
  • Discuss how emerging regulatory trends and new technologies impact the development and lifecycle of medical products
  • Establish various approaches and best practices to promote regulatory reliance in Latin America

Program Committee

  • Maria  Guazzaroni Jacobs, PhD
    Maria Guazzaroni Jacobs, PhD Director, Quality Intelligence, Global Supply
    Pfizer Inc, United States
  • Cammilla  Horta Gomes, MA, MPharm
    Cammilla Horta Gomes, MA, MPharm Latam Regulatory Policy Lead
    Roche, Brazil
  • Livia  Lopes
    Livia Lopes LatAm Regulatory Affairs Policy Manager
    Novartis, United States
  • Michele Aline de Mello, RPh
    Michele Aline de Mello, RPh Regulatory Affairs Manager LATAM, Global Q&R Strategy and Compliance
    Roche Diagnostica do Brasil Ltda, Brazil
  • Maria Cristina  Mota Pina, MBA
    Maria Cristina Mota Pina, MBA Director, Regulatory Policy and Intelligence -Japan, Emerging Markets, Australia
    Latin America Federation of Pharmaceutical Industry (FIFARMA), United States
  • Juliana  Perlow
    Juliana Perlow Director, Regulatory Affairs-CMC, GRACS CMC – Latin America
    MSD, Brazil
  • Ana  Pineda Zavaleta, MSc
    Ana Pineda Zavaleta, MSc International Regulatory Analyst, LAO, OGPS, OPLIA, OC
    FDA, United States
  • Renata De Lima Soares
    Renata De Lima Soares Regulation and Health Surveillance Specialist
    Anvisa, Brazil
  • Sonia  Viejobueno, LLM
    Sonia Viejobueno, LLM US and Latin America Policy Lead, Global Regulatory Policy and Intelligence
    Janssen , Argentina
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Contact us

Registration Questions?

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1.888.257.6457


Exclusive Podcast

Promoting Patient-Centric Business: MedComm in Latin America

Additional Information

Latin America Regulatory Resource Kit

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Regulating Medicines in a Globalized World
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