Page History

This document guide is organized into the following sections:

• Section 1, Introduction, provides an overall introduction to the TIG v1.0.
• Section 2, Fundamentals of the Standard, recaps the basic concepts of models which support the TIG v1.0 and describes how this implementation guide should be used in concert with these models.
• Section 3, Trial Design, describes implementation of standards to represent the design of trials included in a submission.
• Section 4, Product Description, describes implementation of standards to represent data which characterizes a tobacco product.
• Section 5, Nonclinical, describes implementation of standards to represent data from nonclinical studies of tobacco products.
• Section 6, Clinical - Product Impact on Individual Health, describes implementation of standards to represent data from clinical studies to as impact of tobacco products on individual health.
• Section 7, Trial Design Model Datasets (Copy), describes domains for trial-level data, with assumptions and examples.
• Section 8, Representing Relationships and Data (Copy), describes how to represent relationships between separate domains, datasets, and/or records, and provides information to help sponsors determine where data belong in the SDTM.
• guide describing its purpose, organization, and relationship to other CDISC standards and resources.
• Section 2, Standards for Tobacco Product Data, describes how to use CDISC standards and resources for the collection, representation, and exchange of tobacco product data.
• Section 3, Examples, provides examples to demonstrate the intended use of CDISC standards for tobacco product Section 9, Study References (Copy), provides structures for representing study-specific terminology used in subject data.
• Appendices provide additional background material and describe other supplemental material relevant to implementationto support implementation.