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navigating the japan regulatory and clinical trial environment

 February 23, 2012


Location


Online Event
2600 E. Bayshore Road
Palo Alto, California 94303
USA

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.

Who Will Benefit:

This course will be beneficial to:

- Clinical / Pharma & Device personnel
- Clinical Trial Project Managers
- Monitors / CRAs
- QA / QC Personnel
- Pharmacovigilance reporting personnel
- Regulatory personnel whose responsibilities require knowledge of Japan's Regulatory and Clinical Trial environment
- Global Supply Chain personnel
- Manufacturing personnel
- Global Business Development personnel
- All personnel who need to understand the procedures and impact of placing Medical Devices on the Market across the EU

Organized by


ComplianceOnline
2600 E. Bayshore Road
Palo Alto, California 94303
United States of America

More Information


Event's Website



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