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TermDefinition
TA

Therapeutic Area.

The TA is an area of medical practice that encompasses groupings of specific diseases and/or disorders generally treated by a specific medical specialty, such as oncology, cardiovascular, neurology or hematology.

TAPSCTherapeutic Area Standards Program Steering Committee.

CRFs

Case Report Forms.

CRFs used to capture clinical trial data rely on linkages between and among concepts. CRFs also frequently contain logic, such as which values are allowed for a given field, when one field is a value calculated from other fields, and when some fields are not relevant based on an answer to another field

EVS

National Cancer Institute (NCI) Enterprise Vocabulary Services.

EVS provides terminology content, tools, and services to meet the needs of NCI and the biomedical research community.

SMEs

Subject Matter Experts.

 SME is the person who possesses a deep understanding of a particular subject.

TLC

Technical Leadership Committee.

The TLC is made up of Foundational Standards Team Leads. This committee discusses issues pertaining to the Foundational Standards. The TLC also develops the agenda for CDISC IntraChanges and typically leads sessions during these events.

ADaM

Analysis Data Model.  ADaM defines dataset and metadata standards that support: efficient generation, replication, and review of clinical trial statistical analyses, and traceability among analysis results, analysis data, and data represented in the Study Data Tabulation Model (SDTM).​

ADaM is one of the required standards for data submission to FDA (U.S.) and PMDA (Japan).

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Step #RoleInstructions
1.0EVS Terminology Expert / Clinical TA Expert (s)

Gathers CRFs, perform a Public Database Search for existing TA Concepts.

2.0Project TeamEnsure applicable regulatory guidance and requirements are taken into account.
2.1Clinical TA Expert(s)/Project ManagerVerifies that all applicable regulations are taken into account in the standard under development and that such regulatory documents are referenced in the appendix of the standards document.
3.0Clinical TA Expert(s)

Identifies the appropriate core concepts and that the standards under development are aligned with current medical practice and thinking. 

4.0Project ManagerReview scoping materials.
5.0

EVS Terminology Expert

Performs Controlled Terminology Gap Analysis.
6.0ADaM SMEHolds ADaM assessment meeting if applicable.
7.0Project ManagerDraft project charter and project plan.
8.0Project ManagerReview entire scope package with Data Science representative including the expected required Wiki structures.
9.0Project Manager

Submit scoping package to TAPSC/TLC and plans kick-off activities.

10.0TAPSC/TLC

Receives Project Charters(TAs) for approval to proceed with the next stage of the development process.

11.0Project Manager

Posts Project Charter in the team space on the CDISC Wiki.

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