Conducting Clinical Trials in Latin America: keys to successful study implementation

Instructor: Tatiana Vogel
Product ID: 701576
  • Duration: 60 Min

recorded version

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

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: +1-650-565-8542


Read Frequently Asked Questions

This Clinical trial training will review the current status of Clinical Trials activities in Latin America, the factors that make this region such an attractive one and some best practices to ensure a successful implementation of clinical trials.

Why Should You Attend:

Latin America is considered one of the most important emerging markets in Clinical Trials, with a growth rate that by large exceeds the one observed for traditional regions. Over the last 10 – 15 years, Latin America has demonstrated a solid performance as the Regulatory Agencies in most countries have incorporated GCPs as a local requirement, the Clinical Research infrastructure has become stronger and the mass of experienced Investigators has increased.

With all the challenges the Pharma and Biotech Industry is faced today to succeed in a highly competitive environment, Latin America appears as a market with high potential to enable the growth of the Clinical Trials Industry.

This session will focus on reviewing the Benefits as well as the Challenges of managing Clinical Trials in Latin America, offering a detailed description of the Regulatory process and timelines involved for the major contributing countries in the region, while sharing some keys to take into account when conducting clinical trials in the region.

Areas Covered in the Seminar:

  • Overview of the Latin American region.
  • Clinical Trials Activitiy in the Latin American countries.
  • What explains the growth and success of the Region.
  • Regulatory overview of the major contributing countries.
  • Main Challenges in the conduct of Clinical Trials in Latin America.
  • Keys to success in the conduct of Clinical Trials in Latin America.

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 over 14 years of experience managing Clinical Trials; including clinical operations, project management, data management, regulatory expertise and holding a thorough knowledge of the conduct of clinical trials 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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