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FAIRsharing.szrmev; Last edited: April 27, 2021, 8:05 a.m.; Last accessed: Jan 03 2022 7:13 p.m.

Other names: CDISC CT

Names

More detailed information about this field from each metasource.

CDISC Controlled Terminology

metasource: Fairsharing.org
version: FAIRsharing.org: CDISC CT; CDISC Controlled Terminology; DOI: https://doi.org/10.25504/FAIRsharing.szrmev; Last edited: April 27, 2021, 8:05 a.m.; Last accessed: Jan 03 2022 7:13 p.m.

CDISC CT

CDISC Controlled Terminology is the set of codelists and valid values used with data items within CDISC-defined datasets. Controlled Terminology provides the values required for submission to FDA and PMDA in CDISC-compliant datasets. Controlled Terminology does not tell you WHAT to collect; it tells you IF you collected a particular data item, how you should submit it in your electronic dataset.

Description

More detailed information about this field from each metasource.

CDISC Controlled Terminology is the set of codelists and valid values used with data items within CDISC-defined datasets. Controlled Terminology provides the values required for submission to FDA and PMDA in CDISC-compliant datasets. Controlled Terminology does not tell you WHAT to collect; it tells you IF you collected a particular data item, how you should submit it in your electronic dataset.

Webpage:

https://www.cdisc.org/standards/terminology

Webpage

More detailed information about this field from each metasource.

https://www.cdisc.org/standards/terminology

More to explore:

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CDISC Questionnaires, Ratings and Scales

CDISC develops SDTM (tabulation) and ADaM (analysis) QRS supplements that provide information on how to structure the data in a standard format for public domain and copyright-approved instruments. An ...

CDISC Standard for Exchange of Nonclinical Data

CDISC SEND is an implementation of the SDTM standard for nonclinical studies. SEND specifies a way to collect and present nonclinical data in a consistent format.

CDISC Define eXtensible Markup Language

Define-XML transmits metadata that describes any tabular dataset structure. When used with the CDISC content standards, it provides the metadata for human and animal model datasets using the SDTM and/ ...

CDISC Laboratory Data Model

LAB provides a standard model for the acquisition and exchange of laboratory data, primarily between labs and sponsors or CROs. The LAB standard was specifically designed for the interchange of lab da ...

CDISC Analysis Data Model

ADaM defines dataset and metadata standards that support the efficient generation, replication, and review of clinical trial statistical analyses, and traceability among analysis results, analysis dat ...

CDISC Protocol Representation Model

The CDISC Protocol Representation Model (PRM) provides a standard for planning and designing a research protocol with focus on study characteristics such as study design, eligibility criteria, and req ...

DICOM Controlled Terminology

DICOM Controlled Terminology (PS3.16 2017c Annex D)

CDISC Clinical Data Acquisition Standards Harmonization

CDASH establishes a standard way to collect data in a similar way across studies and sponsors so that data collection formats and structures provide clear traceability of submission data into the Stud ...

CDISC Operational Data Model

ODM is a vendor-neutral, platform-independent format (based on XML) for exchanging and archiving clinical and translational research data, along with their associated metadata, administrative data, re ...

CDISC Study Data Tabulation Model

SDTM provides a standard for organizing and formatting data to streamline processes in collection, management, analysis and reporting. Implementing SDTM supports data aggregation and warehousing; fost ...

CDISC Study/Trial Design Model

The CDISC Study/Trial Design Model in XML (SDM) is an extension of ODM and enables organizations to provide rigorous, machine-readable, interchangeable descriptions of the designs of their clinical st ...

CDISC Clinical Trial Registry XML

CTR-XML lets technology vendors implement tools that support a "write once, use many times" solution based on a single XML file that holds the information needed to generate submissions for multiple c ...

CDISC Glossary

CDISC Glossary seeks to harmonize definitions (including acronyms, abbreviations, and initials) used in the various standards initiatives undertaken by CDISC in clinical research. Glossary also serves ...

CDISC Dataset-XML

Dataset-XML supports exchanging tabular data in clinical research applications using ODM-based XML technologies, enabling the communication of study datasets for regulatory submissions.

INCENTIVE Community Controlled Vocabulary

Controlled vocabularies allow an accurate and controlled approach in describing physical and digital assets (e.g., data). One of such controlled vocabulary is INCENTIVE Controlled Vocabulary. This con ...

DATACITE V4.4

Controlled vocabularies allow an accurate and controlled approach in describing physical and digital assets (e.g., data). One of such controlled vocabulary is Datacite Controlled Vocabulary. This cont ...

Pathway Terminology System

Pathwas terminology systems integrates biological Events and various Pathway types.

Biomedical Research Integrated Domain Group Model

BRIDG is a domain analysis model that represents the realm of protocol-driven clinical, pre-clinical, translational and basic research. This breadth includes concepts from Common (i.e., concepts share ...

Minimal Anatomical Terminology

A minimal set of terms for anatomy.

NCI Thesaurus

NCI Thesaurus (NCIt) provides reference terminology for many NCI and other systems. It covers vocabulary for clinical care, translational and basic research and public information.

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Data is amalgamated and only retrieved periodically.
Some of the resources used by the system:

® FAIRsharing.org
® Bioontology/Bioportal Terms
® Nucleic Acid Research - Database
® re3data.org
® bio.tools
® PubMed - Courtesy of the U.S. National Library of Medicine