ComplianceOnline

Outsourcing Clinical Trials in Latin America

Instructor: Tatiana Vogel
Product ID: 701690
  • Duration: 42 Min

recorded version

$249.00
1x Person - Unlimited viewing for 6 Months
(For multiple locations contact Customer Care)
Recorded Link and Ref. material will be available in My CO Section

Training CD

$450.00
One CD is for usage in one location only.
(For multiple locations contact Customer Care)
CD and Ref. material will be shipped within 15 business days

Customer Care

Fax: +1-650-963-2556

Email: customercare@complianceonline.com

Read Frequently Asked Questions

This clinical trial training will review some Outsourcing Models that have been used successfully in the Latin American countries where Clinical Research is developed, identifying best practices and opportunities that speed protocol approval in these countries.

Why Should You Attend:

Latin America is one of the top emerging markets in Clinical Trials, showing double digit growth in the number of studies it executes, high enrollment rates and quality levels comparable or better that those shown by sites in the US. One key factor that has enabled the success of the region has been the Outsourcing models implemented, which range from Specific Functional Service Providers to Full Service Providers.

This session will review different Outsourcing Models in Clinical Research available within the Latin American Region, covering Clinical Research Operations; Central Laboratories and Logistics. Achieving a better understanding of the capabilities of the region in terms of Clinical Research Service Providers will facilitate decision making and enable to identify opportunities for increased efficiency in the implementation of Clinical Trials in the region.

Areas Covered in the Seminar:

  • Overview of the Latin American region.
  • Clinical Trials Activitiy in the Latin American countries.
  • Outsourcing Capabilities for Clinical Research In Latin America.
  • Review of available outsourcing providers and their service options.
  • Opportunitites for Increased efficiency.
  • Succesful outsourcing models.

Who Will Benefit:

This session will provide valuable assistance to the Pharmaceutical, Biotech and CRO Businesses involved in the management of clinical trials, with interest in expanding their activitiy to Latin America, including representatives such as:

  • Research Directors
  • Clinical Study Managers
  • Regulatory Affairs Directors/Managers
  • Project Directors/Managers

Instructor Profile:

Tatiana Vogel, Ph., is a Clinical Research Consultant with 15 years of experience managing Clinical Trials; including clinical operations, project management , data management and regulatory in the leading countries in Latin America.

Tatiana provides clinical trials Consulting Services to several CROs in Latin America and was formerly Assoc. Director of Research Operations in Latin America for Merck & Co.

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