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Fri - Dec 9, 2011 @ 09:00 AM CST Ended
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South Korea: Navigating the Regulatory and Clinical Trial Environment

(complianceonline.com)

This 6-hr virtual seminar will focus on the regulatory compliance requirements and procedures for conducting Clinical Trials on Pharmaceutical Products 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.

NOTE : Use this Promocode (128600) to avail 10% discount, valid upto 7th December 2011.

Tags

  • South Korea Regulatory Compliance, Clinical Trial Requirements, Regulatory Structure in South Korea, KFDA regulations, Drug Development Process, South Korea CRO selection, IMD, Clinical Trials in Sout

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