5th Latin America Clinical Trials

 3 DAYS OF SESSIONS

 28 SPEAKERS

 15 NETWORKING OPPORTUNITIES

 Over 100 ATTENDEES...

...AND GROWING!

 

NEW ADDED TALK!
 

PANEL
Ethical Considerations: Are Clinical Trials an Alternative to Medical Care in Latin America? Examining the Ethical Factors Behind  Clinical Research in Latin America 

Moderated By:

Mario Boskis, M.D., Director, Clinical Trial Department, Activa-CRO

Panelists Include:

Gabriel Zeitune, M.D., Director, Biostarting (former Director, DEMA, ANMAT)

Fernando Martinez, PhD, MBA, Executive Director of Global Operations, inVentiv Clinical Solutions LLC

Daniel Goldenberg, M.D., FCP, Director, Comité de Ética para Investigaciones Clínicas, Asociación Argentina de Investigaciones Ética

Fabian Dabove, M.D., Clinical Research Manager, Genzyme Argentina S.A.

 

ExL Pharma is pleased to present its 5th Latin America Clinical Trials conference continuing the ongoing discussion of the opportunities and difficulties for conducting clinical research within the Latin America region.  The continents’ experts will be sharing updates and best practices on topics such as clinical trial quality, drug access, regulatory and ethical committee changes and other critical issues that the pharmaceutical industry is facing today.

In addition, the agenda this year will feature a one-day seminar geared toward the project management professional that will provide insight into the key aspects of running a clinical research project with special consideration for quality assurance and nurturing high-quality research sites.

We look forward to another successful program this August and hope you can join us in Buenos Aires!


Matthew MillmanVisite nuestra  pagina web en español
Conference Director
mmillman@exlpharma.com

Kristen Hunter
Team Leader, Production
ExL Pharma

Who should Attend

This Summit is specifically designed for C-Levels, Department Heads, Vice Presidents, Directors and Managers at pharmaceutical, biotechnology and medical device companies from the following departments:

  • Scientific and Medical Directors/Affairs
  • Regulatory Affairs and Liasons
  • Clinical/R&D Operations, Research
  • Clinical Quality Assurance/Control
  • Clinical Outsourcing -- Planning and Vendor Management
  • Strategic Business Development/Operations
  • Project/Study Management/Project Planning
  • Clinical Trial Capacity Planning/Management
  • Clinical Trial Process Improvement/Enhancement
  • Clinical Compliance
  • Clinical Safety
  • Patient Recruitment/Clinical Trial Enrollment