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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 collected study data using the Study Data Tabulation Model (SDTM); , and
  • Creation creation of analysis datasets using the Analysis Data Model (ADaM), with
  • references to additional CDISC standards and resources to support implementation.

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.

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