This webinar on conducting clinical trials in Latin America will provide examples of work flow for obtaining approval including Regulatory steps, documentation requirements and associated timelines. Attendees will be able to differentiate the work flow depending on the type of study and country regulatory systems and identify common requirements and expectations that are applicable across all analyzed countries. The varying methods of obtaining Informed Consent in the analyzed countries will be described. Challenges and Opportunities entailed in the implementation of Clinical Research in the Region will be addressed taking into consideration different cultures and the way their people communicate when conducting Clinical Research. The clinical study drivers that attract studies into Latin America will be discussed.
Distinguish the different regulatory processes and timelines for setting up clinical studies in Latin America (Brazil, Mexico, Argentina and Chile).
Identify and respond in advance to challenges associated to the countries and the region when planning a study.
Differentiate ways of communicating associated to cultures in the region.
CEO - Development Strategy and Quality Assurance,
Blanchad & Asociados - LATINABA
Webinar Replay: An Overview: How To Set Up Studies in Latin America Exam
1.00 - ACRP Credits
1.00 - CME Credits
1.00 - CNE Credits
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