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Overview

DIA brings you a symposium with interactive dynamics, where you will engage 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.

We will be translating:

  • English to Spanish and Portuguese
  • Spanish to English and Portuguese
  • Portuguese to English and Spanish

LETTER TO SUPPORT YOUR US VISA APPLICATION
DIA can provide a letter to confirm your onsite participation as long as you have:

  • Already registered for this conference and
  • Paid the registration for this conference

To request a confirmation letter please send an email to Megan Stevens at Megan.Stevens@diaglobal.org.



On-Demand Content Preview Webinar

The US FDA Generic Drug Program – The Framework to "Sameness"
Gain an overview of the legal framework for how generic drugs can be developed for approval in the United States, and more.
Register today.

New Podcast!

Promoting Patient-Centric Business: MedComm in Latin America
Hear Barbara Nardi, Associate Director of Medical Communications, PPD, Brazil, and Emanuela Lopes Fernandes Saraiva, Customer Service and Medical Information Manager in Pharmacovigilance, Libbs Farmaceutica, Brazil, discuss topics from DIA's Latin America Medical Information and Communication Workshop.
Listen in.

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 conclusion of this conference, participants should be able to:

  • Discuss various initiatives related to global regulatory convergence and harmonization and their impact on the access of medicines and future R&D in Latin America
  • Examine various approaches and best practices to ensure regulatory reliance in Latin America

Program Committee

  • Mario  Alanis
    Mario Alanis General Director of International Affairs
    Federal Commission for the Protection against Sanitary Risks (COFEPRIS), Mexico
  • Peter  Baker
    Peter Baker International Relations Specialist, OIP, OGROP
    FDA, United States
  • Maria  Guazzaroni Jacobs, PhD
    Maria Guazzaroni Jacobs, PhD Director Quality and Regulatory Policy (QRP), Pfizer Global Supply
    Pfizer Inc, United States
  • Maria Cristina  Mota Pina, MBA
    Maria Cristina Mota Pina, MBA Director, Regulatory Policy and Intelligence -Japan, Emerging Markets and Austra
    AbbVie, Inc., United States
  • Jaime  Oliveira, DrPH, AHIP
    Jaime Oliveira, DrPH, AHIP Head Regulatory Policy and Intelligence LatAm
    Bayer S.A., Brazil
  • Patrícia  Oliviera Pereira
    Patrícia Oliviera Pereira Head, Office of International Affairs
    Brazilian Health Surveillance Agency - ANVISA, Brazil
  • Ana  Padua, MSc, RPh
    Ana Padua, MSc, RPh Associate Director GRA CMC Regulatory Intelligence Biopharam Global Regulatory
    EMD Serono, Switzerland
  • Ana Patricia  Pineda, MSc
    Ana Patricia Pineda, MSc International Regulatory Analyst, OIP, OGROP, OC
    US FDA, Mexico
  • Analia  Porras
    Analia Porras Unit Chief, Medicines and Health Technologies
    Pan American Health Organization (PAHO), United States
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Contact us

Registration Questions?

Send Email
1.888.257.6457


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