Meet Regulatory Requirements and Effectively Manage and Train Sites
- Lima, Peru
Last September, our inaugural conference convened key stakeholders involved with clinical trials in Latin America. As Latin America is an increasingly desirable location for running clinical trials, and it is important for those involved to collaborate with colleagues and industry counterparts regarding the challenges of developing, executing and completing clinical trials in Latin America.
This is a unique opportunity for pharmaceutical executives in Latin America to hear from key regulatory officials, pharmaceutical leaders, CROs and sites on how all stakeholders in the clinical process can ultimately achieve desired results.
This is an exceptional opportunity to improve upon clinical trials in this important market.
Topics being researched for 2011 include:
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The Regulatory Framework — Hearing From Key Regulatory Stakeholders when Designing Clinical Trial Protocols
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Ethical Considerations when Conducting Clinical Trials in Latin America
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Matching Clinical Trial Protocol to Appropriate Sites
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Enhancing the Latin American Image in the United States
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Logistical Issues and Clinical Project Management
For more information or to register, please contact the Center for Business Intelligence toll free by phone at 1-800-817-8601 or via e-mail at cbireg@cbinet.com.
