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The TIG guides implementation of CDISC models to standardize collection, representation, and exchange of tobacco product data. CDISC models implemented in this guide include:

• CDASH Model Version 1.2, which provides a general framework for creating fields to collect information on CRFs
• SDTM Version 2.1, which provides a standard model for study data tabulations
• ADaM Version 2.1, which specifies the principles and standards to follow in the creation of analysis datasets and associated metadata

CDISC foundational standards are available at https://www.cdisc.org/standards.

The TIG also references additional standards and resources to support implementation:

• CDISC Controlled Terminology (available at https://www.cdisc.org/standards/terminology/controlled-terminology) provides consistent semantics for use across standards.
• The CDISC Non-standard Variables Registry (available at https://www.cdisc.org/standards/terminology/non-standard-variables) serves as a reference for using or creating NSVs, to drive consistency in implementing CDISC Standards.
• CDISC QRS supplements (available at https://www.cdisc.org/foundational/qrs) provide information on how to structure data in a standard format for public-domain and copyright-approved instruments.
• TIG Conformance Rules Version 1.0 (available at <placeholder, link pending>)

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  support the assessment of tabulation and analysis datasets' conformance to TIG standards.
• The CDISC eCRF Portal (available at https://www.cdisc.org/kb/ecrf) provides a platform from which to download standard CRFs, including metadata standardized per the Operational Data Model (ODM, available at https://www.cdisc.org/standards/data-exchange/odm). ODM is a vendor-neutral, platform-independent format for representing and exchanging CRF content in electronic data capture (EDC) tools.
• The CDISC Library (https://www.cdisc.org/cdisc-library) provides access to information regarding new relationships between standards as well as a number of versioned CDISC standards and controlled terminology packages.
• CDISC Define-XML Version 2.1 (

TIG v1.0 provides specific domain models, assumptions, business rules, and examples for preparing standard data collection, tabulation datasets, and analysis datasets that are based on the CDASH, SDTM, ADaM, and Analysis Results models respectively. This document is intended for companies and individuals involved in the collection, preparation, and analysis of product description, non-clinical, and clinical data that will be submitted to regulatory authorities. The TIG should be used with:

• Version 1.2 of the CDISC Clinical Data Acquisition Standards Harmonization (CDASH, available at https://www.cdisc.org/standards/foundational/cdash/cdash-model-v1-2), provides a general framework for creating fields to collect information on CRFs and includes the model metadata, which shows the standard variables in the model.Version 2.0 data-exchange/define-xml/define-xml-v2-1) provides a metadata standard used to describe any tabular dataset structure.
• Education curriculum (available at <placeholder, link pending>)

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   to support understanding and use of the TIG v1.0.

The TIG is a stand-alone implementation guide and is not intended to be inherently related to or dependent on other implementation guides published by CDISC. However, to support alignment across implementation approaches and for efficiency, the TIG was developed in part by leveraging content published in other CDISC implementation guides. Given this, implementers familiar with CDISC documents may recognize alignment and content shared between the TIG and the following guides:

• Version 3.1.1 of the Standard for Exchange of Nonclinical Data Implementation Guide: Nonclinical Studies (SENDIG; of the CDISC Study Data Tabulation Model (SDTM, available at https://www.cdisc.org/standards/foundational/sdtm), which describes the general conceptual model for representing clinical study data that is submitted send/). SEND guides the organization, structure, and format of standard nonclinical tabulation datasets for interchange between organizations such as applicants and contract research organizations (CROs), and for submission to regulatory authorities.
• Version 2.1 2 of the CDISC Analysis Data Model (ADaM, availble at ), which describes...
• Version TBD of the Analysis Results Model... 
• Version 2.0 ODM-XML
• Version 1.0 Lab-XML
• CDASH Implementation Guide (CDASHIG; available at https://www.cdisc.org/standards/foundational/cdash/). The CDASHIG defines basic standards for the collection of clinical trial data and describes how to implement the CDASH model for specific CRFs.
• Version 3.4 of the SDTM Implementation Guide: Human Clinical Trials (SDTMIG; available at https://www.cdisc.org/standards/foundational/sdtmig/). The SDTMIG is intended to guide the organization, structure, and format of standard clinical trial tabulation datasets used for various purposes, including publication, warehousing, meta-analyses, and regulatory submission.
• Version 1.3 of the of the ADaM Implementation Guide (ADaMIG; available at https://www.cdisc.org/standards/foundational/adam/). The ADaMIG specifies ADaM standard dataset structures and variables, including naming conventionsVersion 2.1 Define-XML...