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Electronic Common Technical Document (eCTD)
Course Summary
The eCTD is mandatory for all applications for marketing approval and all subsequent related submissions in the European Economic Area, the USA and Canada. Other countries intend to make its use mandatory. The eCTD specification has been developed to facilitate the global electronic submission, review and lifecycle management of medicinal product dossiers for regulatory applications. It broadens the scope of the CTD to include information on variations, renewals and amendments, so that it is no longer a static document but is updatable throughout the life of the product. This module outlines the eCTD specification, discusses the approach to regional differences in dossiers, and provides guidance on creation of an eCTD submission. The module provides a training and reference tool that will be of particular value to those new to the use of the format.
Purchasing Information
When you have completed your course order, Zenosis will finalise the setup of your course materials and contact you on the email address that you provide in your order. You can expect this process to be completed within one business day (using the UK business calendar) of completing your payment.
It is therefore essential that you use your real email address for your order, or indicate in the purchase notes the email address to be used for the course set-up, and check that any messages from Zenosis or grapl are not lost in your junk or spam folder.
You will have access to the course module(s) for a period of 180 days after your purchase is complete.
Detailed Course Information
Learning Objectives
• Describe the structure, requirements and functionality of the eCTD.
• Outline XML basics and the architecture of the eCTD.
• Discuss Document Type Definitions (DTDs) and schemas.
• Explain how to build an eCTD.
• Specify regional differences.
• Discuss life cycle and change management.
• List criteria that will make an electronic application technically valid.
• Initiate electronic transfer to a regulatory authority.
• Create, submit and maintain an eCTD dossier throughout the life of a drug product.
Who will benefit from this course
This module is an essential tool for regulatory affairs and compliance staff and specialists in data handling, knowledge management or documentation. All those involved in drug development and who contribute to regulatory submissions will also wish to familiarise themselves with its contents.
Module Outline
• Introduction
– This session defines the eCTD and identifies advantages of using this submission format.
• Technical infrastructure
– This session gives information on XML specification and style sheets and describes the eCTD backbone.
• Directory structure
– This session looks at the eCTD hierarchy, life cycle management and structure of the five modules.
• Creating an eCTD submission
– This session explores the workflow around planning, creating and submitting an eCTD – particularly setting up the modules, and migrating and validating the data.
• Special components
– Features of the Canadian, EU, Japanese and US DTDs/schemas and the STF specification are outlined.
• Tools
– This session includes a case study and an eCTD checklist to assist learners when compiling an eCTD submission.
• Assessment
– Multiple-choice mastery assessment.
Roles
Regulatory
CPD Points
2.5
Region
Level
Introductory/Intermediate
Course Study Time
Approx 2.5 hours
USA, Europe, Other