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Introduction to Japanese Institutions and Regulatory Authorities

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Overview 

The course, a Thomson Reuters Cortellis Regulatory Online Learning module, describes the structure and organization of Japan’s government institutions and its lawmaking process. It explores the functions, structure, and responsibilities of the Ministry of Health, Labor and Welfare (MHLW) and of the Pharmaceutical and Medical Devices Agency (PMDA). The course reviews key Japanese pharmaceutical legislation and provides an overview of the new drug application (NDA) review process. The course concludes with a review of cultural considerations that will help learners better understand Japan’s business code and practices.

Featured Topics 

  • Japanese pharmaceutical legislation
  • Japan’s MHLW
  • Japan’s PMDA
  • Japan’s business code and practices

Who Should Attend 

Professionals and experts in the pharmaceutical, biotechnology, and medical device fields

Learning Objectives 

Participants who complete this course should be able to:

  • Describe the structure and organization of the Japanese government
  • Outline the lawmaking process
  • Identify the functions and organization of the Ministry of Health, Labor and Welfare
  • Examine the role of the Pharmaceutical and Medical Devices Agency
  • Review the history of pharmaceutical legislation
  • Analyze the New Drug Approval Process
  • Understand the code of business conduct in Japan

The course takes an average of two hours to complete.

Contact Information 

Linda Belmont, DIA
Phone +1.215.293.5818
Linda.Belmont@diahome.org

Technical Requirements 

Click here for minimum system requirements.

Registration Fees 

Other Fees

Individual
$360.00
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Unless otherwise disclosed, the statements made by speakers represent their own opinions and not necessarily those of the organization they represent, or that of the Drug Information Association. Speakers, agenda and CE information are subject to change without notice. Recording of any DIA educational material in any type of media is prohibited without prior written consent from DIA.

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