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Preparing Submissions in the Common Technical Document (CTD) Format
Course Summary
The CTD is the internationally recognised standard format for submissions to medicines regulatory authorities. In the European Economic Area, the USA and Canada, the CTD, in its electronic format (eCTD), is mandatory for all applications for marketing approval and all subsequent related submissions. The CTD is accepted in many other countries, being mandatory for new prescription medicines in some. This module explains the rationale for the CTD and provides guidance on its structure and format and the ways in which it is used.
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
• Explain the rationale for the CTD, and describe the ways in which it is used.
• Identify regional differences in regulatory requirements for information in a CTD-formatted submission.
• Describe the structure of the CTD.
• Access guidance on detailed structure and content of the CTD.
• Outline formatting requirements for a CTD dossier.
Who will benefit from this course
Regulatory affairs and compliance staff, and all those involved in drug development and who contribute to regulatory submissions, will find the module an invaluable introductory training course and/or a useful reference tool. Specialists in data handling, knowledge management or documentation will also wish to familiarise themselves with its contents.
Module Outline
• Introduction
– This session introduces you to the nature of the Common Technical Document (CTD), a global standard designed by the ICH (International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use). The composition of a regulatory submission team is outlined.
• High-level structure
– In this session you will become more familiar with the five modules of the CTD.
• Fine structure and format
– You will be given access to guidelines that specify in detail the structure of each module of the CTD and the relationship between their sections and the documents that make up a dossier. Recommendations are also given on how to segregate and paginate documents and how to format pages, tables of contents and cross-references.
• Using the CTD
– Different ways in which you can use the CTD in practice are described.
• Assessment
– Multiple-choice mastery assessment.
Roles
Regulatory
CPD Points
1.5
Region
Level
Introductory/Intermediate
Course Study Time
Approx 1.5 hours
USA, Europe, Other