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The purpose of the TIG is to guide the use of CDISC standards for the organization, structure, and format of tobacco product study data submitted to a regulatory authority. The TIG provides guidance for the:

• Collection collection of study data with case report forms (CRFs) using the Clinical Data Acquisition Standards Harmonization (CDASH) model;,
• Tabulation tabulation of study data using the Study Data Tabulation Model (SDTM);, and
• Creation creation of analysis datasets using the Analysis Data Model (ADaM); , with
• References references to the:
• CDISC eCRF Portal and related Operational Data Model (ODM-XML) standards
Define-XML additional CDISC standards and resources to support the exchange of structured data between parties and across different information systemsimplementation.
• CORE

The TIG also provides examples for use cases inherent to tobacco product studies to demonstrate and support understanding of the intended use of these standards.