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Pennsylvania Convention Center

2016年6月26日 (日) 午前 8:30 - 2016年6月27日 (月) 午後 12:00

1101 Arch Street, , Philadelphia, PA 19107 , USA

DIA Latin America Regulatory Conference (LARC) 2016

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

概要

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 conference with interactive dynamics, where you will be engaged in discussions with key stake holders influencing the advancement and implementation of regulatory convergence initiatives in Latin America.

The focus of this year’s LARC will be on regulatory evolution, multi-regional cooperation, global harmonization, and best practices. Sessions will highlight regulatory approaches and good practices to ensure reliance in Latin America, strategic initiatives to improve collaboration and cooperation, and the changing landscape of CMC in Latin America.


Live translation will be available in Español.
View English and Español versions of the program.

View Speaker Biographies & Disclosures


特集トピック

  • Regulatory Convergence
  • Harmonization Initiatives and Best Practices
  • Pan-American Network for Drug Regulatory Harmoniztion (PANDRH) Strategic Plan
  • Regulatory Cooperation and Reliance
  • Quality CMC/Harmonization

 

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Want to learn more about DIA Latin America Regulatory Conference (LARC) 2016? You've come to the right site!

Continuing-Education

参加対象

This conference will benefit individuals involved in:

  • Drug regulation
  • Clinical research and development
  • Medical and scientific affairs
  • Quality assurance
  • Research and development
  • Strategic sourcing/planning
  • Regulatory affairs

学習目的

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 research and development in Latin America
  • Examine various approaches and best practices to ensure regulatory reliance in Latin America
  • Describe challenges in Latin America in areas related to quality/CMC

プログラム委員会

  • Justina  Molzon, JD, MS
    Justina Molzon, JD, MS Consumer Services
    Consumer Services, United States
  • Mike  Ward
    Mike Ward Coordinator, Regulatory Systems Strengthening, EMP
    World Health Organization (WHO), Switzerland
  • Maria  Guazzaroni Jacobs, PHD
    Maria Guazzaroni Jacobs, PHD Director, Quality Intelligence, Global Supply
    Pfizer Inc, United States
  • Ana  Padua, MSC, RPH
    Ana Padua, MSC, RPH Director EU Global Regulatory and Scientific Policy
    Merck Kgaa, Darmstadt, Germany (EMD Serono, US), Switzerland
  • Patricia  Oliveira Pereira Tagliari, LLM, MPH
    Patricia Oliveira Pereira Tagliari, LLM, MPH Associate Director of the Second Directorate
    ANVISA, Brazil
  • Ivana R. Antonacci, MS
    Ivana R. Antonacci, MS Global Regulatory Consultant
    United States

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