The SDTM establishes a standard way to tabulate data across studies.
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Guidance in this section
supports and provides implementations of the SDTM to represent data to characterize products, data to identify potential risks and effects on biological processes for products via in vitro and in vivo nonclinical studies, and data to assess the impact of products on the health of individuals. The CDISC Standards implements the SDTM for TIG Product Description, Nonclinical, and Product Impact on Individual Health use cases. TheCDISCStandard for Exchange of Nonclinical Data (SEND) is a specialized approach to implement the SDTM for nonclinical research. Guidance for nonclinical use cases in this this section reflects implementation of the SDTM per SEND. Implementation of the SDTM is simply referred to as "SDTM" for all other use cases in this section.All tables in this section begin with column Num. Values in Num are consecutive numbers intended only to support ease of use (e.g., to allow implementers to reference rows in tables without describing row contents). Values in Num have no meaning beyond this use.