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.
Featured
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
- 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 • Director, Quality Intelligence, Global Supply
Pfizer Inc, United States -
Cammilla Horta Gomes, MA, MPharm • Latam Regulatory Policy Lead
Roche, Brazil -
Livia Lopes • LatAm Regulatory Affairs Policy Manager
Novartis, United States -
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 • Director, Regulatory Policy and Intelligence -Japan, Emerging Markets, Australia
Latin America Federation of Pharmaceutical Industry (FIFARMA), United States -
Juliana Perlow • Director, Regulatory Affairs-CMC, GRACS CMC – Latin America
MSD, Brazil -
Ana Pineda Zavaleta, MSc • International Regulatory Analyst, OIP, OGROP, OC
FDA, United States -
Renata De Lima Soares • Regulation and Health Surveillance Specialist
Anvisa, Brazil -
Sonia Viejobueno, LLM • Latin America Lead, Global Regulatory Policy and Intelligence
Janssen , Argentina
Contact us
Registration Questions?
Exclusive Podcast
Promoting Patient-Centric Business: MedComm in Latin America
Additional Information
Latin America Regulatory Resource Kit
On Demand Content Preview Webinar
Regulating Medicines in a Globalized World
Register Today!
