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Clinical Project Management Training

Nov 7 2013 8:00AM - Nov 7 2013 5:00PM | Crowne Plaza WTC Hotel Dakota 95 Col. Napoles Del. Cuauhtemoc Mexico City 03810 Mexico

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Who Should Attend 

Professionals involved in:

  • Clinical research and development
  • Quality assurance
  • Regulatory affairs
  • Clinical supplies
  • Data management
  • SOP administration
  • Clinical site operations

Learning Objectives 

  • Define the scope of interventional and observational clinical studies
  • Understand and differentiate clinical research phases
  • Portray main features of study design
  • Comprehend global regulatory framework and its application to accomplish a successful clinical study
  • Recognize the contribution of the inclusion of Latin American Patients in a global drug development
  • Evaluate the influence of ethnicity in a clinical development
  • Anticipate ethical concerns during the conduction of clinical trials in Latin America
  • Define the study scope, evaluate main requirements and identify suppliers for a feasible conduction of a clinical trial
  • Create quality systems for clinical trials
  • Plan and manage communication between investigators, monitors and authorities

Contact Information 

For further information:

Washington, DC
Mr. Alejandro Bermudez-Del-Villar, MA/IBBD
Latin American and Global Development Coordinator

Mr. Arturo Rodriguez
President, ACROM
Tel. (55) 50 80 36 20


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