3-hr Virtual Seminar: South Korea - Navigating the South Korean Regulatory Compliance and Clinical Trial Environment

This 3-hr training on South Korean regulatory compliance requirements for life science products will discuss about the regulatory structure, clinical trial requirements and the conduct of running clinical research in South Korea.

Why Should You Attend:

This 3-hr session will help you gain a understanding of the regulatory structure, clinical trial requirements and the conduct of running clinical research in South Korea. It will prepare you for the regulatory approval processes, Agency meetings, the complexities of running studies in South Korea, the importance of partner selection and the cultural knowledge needed for success. The recent changes made by KFDA to be more sponsor-friendly will be reviewed. Real world experiences on actual interactions with the Agency since the changes, will also be discussed.

Note: A detailed, 6-hr training is available on the same topic. Click here to purchase that training

Event Details:

Date: November 09, 2012
Time: 09:00 AM-12:00 PM PDT
Cost: $399 per attendee per computer terminal
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For Registration:

http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=702153?channel=worldconf