Webinar: Regulatory Requirements of Japan

Webinar: Regulatory Requirements of Japan
This webinar will discuss regulatory requirements in Japan


Date: 18th July 2017
Time: 3pm-4pm (BST)







This webinar will cover key topics, including: 

  • Strategic considerations for the Japanese market
  • General regulatory requirements for clinical trials in Japan
  • Preparation for PMDA scientific advice
  • Cultural considerations

Who should attend?

This webinar will be suitable for all individuals as it will start with the basic introduction of the Japanese regulatory framework, 

Why you should attend

During this webinar you will learn about the regulatory requirements for Japan focusing on the key elements which are very different from the EU regulatory practices, including clinical trials and preparing for PMDA scientific advice. This will provide you with the essential updated tools for forming your Japan and Global Regulatory strategies and discuss the cultural differences when working with Japanese companies. 
 

CPD

This course offers 1 CPD hour for successful completion, to learn about why CPD is important visit the Lifelong Learning page.

Cost of the webinar

Members: £75.00 + VAT
Non members: £95.00 + VAT
All prices are in pounds sterling and are exclusive of VAT

To register, please log in or create an account 

Please read the training terms and conditions before booking this course. By booking a place on this course you are agreeing to the training terms and conditions.


 
When
11/07/2017
Where
At Your Desk
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NOTE
Important instructions before booking - If your company name or VAT number does not appear here or you would like to be invoiced using a different VAT number, please email finance@topra.org

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