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Navigating the Japan Regulatory and Clinical Trial Environment; Conducting Clinical Studies in Japan
| Date |
Jul 13, 2012 07:00 AM
Ending : Jul 13, 2012 01:00 PM
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| Event Type |
Online Webinar,
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| Link to Website/Contact |
http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=702170?channel=BostonEL |
| Phone |
16506203915 |
| Location |
2600 E. Bayshore Road Palo Alto California 94303 |
| Organizer |
ComplianceOnline |
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Description:
This Japan Regulatory and Clinical Trial Requirements training will cover Japan Regulatory Agency Structure and Responsibilities, its review process for decision-making and approval, requirements for clinical trials in Japan and the procedures for conducting clinical studies in the country and reporting them.
Why Should You Attend:
This 6 hour virtual seminar will help you gain a comprehensive understanding of the Regulatory Structure, Clinical Trial Requirements and the Conduct of Running Clinical Research in Japan. It will prepare you for the regulatory approval processes, Agency meetings, the complexities of running studies in Japan, the importance of partner selection and add the cultural knowledge needed for success. The recent changes made by PMDA to be more sponsor-friendly will be reviewed. Real world experiences on actual interactions with the Agency since these changes, will also be discussed.
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Tags :
compliance training
online compliance training
compliance training program
regulatory compliance training
corporate compliance training
fda compliance training
