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Overview of the CTD and eCTD

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The course, a Thomson Reuters Cortellis Regulatory Online Learning module, describes the Common Technical Document (CTD) and the electronic Common Technical Document (e-CTD).  The course introduces learners to the CTD by covering its goals and its impact on drug sponsors. The course explores the structure of the CTD, detailing the content and granularity for each of the five modules. It concludes with a review of the eCTD that covers specifications, scope, implementation, architecture, functional requirements, and checksums.

Featured Topics 

CTD and E-CTD and the impact on drug sponsors

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:

  • Explain the goal of the CTD
  • Describe the impact the CTD has had on applicants and sponsors
  • Recognise the information contained in each module of the CTD
  • Understand the granularity of each CTD module
  • Describe the purpose of the eCTD specifications
  • Define the scope of the eCTD
  • Identify key eCTD implementation dates
  • Understand the functional requirements of the eCTD

The course takes an average of one hour to complete.

Contact Information 

Linda Belmont, DIA
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Technical Requirements 

Click here for minimum system requirements.

Registration Fees 

Other Fees

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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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