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FDA Compliance 2012 - South Korea: Navigating the Regulatory and Clinical Trial Environment
Date2012-03-01
Deadline2012-03-01
VenuePalo Alto, USA - United States 
KeywordsSouth Korea Regulatory Compliance; Clinical Trial Requirements; Regulatory Structure in South Korea; KFDA regulations; Drug Development Process; South Korea CRO selection
Topics/Call fo Papers
This 6-hr virtual seminar will focus on the regulatory compliance requirements and procedures for conducting Clinical Trials on Pharmaceutical Products in South Korea. It will also cover topics relating to pre-clinical and clinical requirements and address the structure of the regulatory agencies in South Korea.
Why Should You Attend:
This 6-hr training will provide valuable insights into how regulations and compliance issues are culturally handled in Japan.
This course specifically focuses on the regulatory compliance requirements and procedures for conducting Clinical Trials on Pharmaceutical Products in Japan.
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Last modified: 2011-12-26 17:30:08