Clinical Data Interchange Standards Consortium
Encyclopedia
Clinical Data Interchange Standards Consortium (CDISC) is a non-profit organization
, whose mission is "to develop and support global, platform-independent data standards that enable information system interoperability to improve medical research and related areas of health-care". Their main project, the described data standard, bears the same name. The data standards are defined as a series of Models, which can be expressed using an underlying electronic format. The preferred electronic format is XML, using the Operational Data Model (ODM) as a base XML Schema.
CDSIC registered solutions providers
MetaData only import allows only the importing of MetaData. This is useful for setting up the EDC system to capture data. Basically allows third party software to define the forms, variables etc. used in the EDC system. This provides a EDC vendor-neutral system for defining a study.
Non-profit organization
Nonprofit organization is neither a legal nor technical definition but generally refers to an organization that uses surplus revenues to achieve its goals, rather than distributing them as profit or dividends...
, whose mission is "to develop and support global, platform-independent data standards that enable information system interoperability to improve medical research and related areas of health-care". Their main project, the described data standard, bears the same name. The data standards are defined as a series of Models, which can be expressed using an underlying electronic format. The preferred electronic format is XML, using the Operational Data Model (ODM) as a base XML Schema.
CDISC History
- Late 1997 - Started as a Volunteer group
- Summer 1998 - Invited to form DIA SIAC
- Feb 2000 - formed an Independent, non-profit organization
- Dec 2001 - Global participation
CDISC standards
- Study Data Tabulation Model (SDTMSDTMSDTM defines a standard structure for human clinical trial data tabulations that are to be submitted as part of a product application to a regulatory authority such as the United States Food and Drug Administration...
)- Highlights: recommended for FDA regulatory submissions since 2004.
- Study Data Tabulation Model SDTM Implementation Guide (SDTM-IG)
- Gives a standardized, predefined collection of submission metadata "Domains" containing extensive variable collections.
- Analysis Data Model (ADaM)
- Designed to complement the SDTM submission by detailing the statistical analysis performed on the clinical trial results.
- Standard for Exchange of Non-clinical Data (SEND)
- The animal trial equivalent of SDTM.
- Operational Data Model (ODM)
- The highlights of ODM: includes audit trail, utilizes XML technology, machine- and human- readable, all information are independent from databases, storing of ODM is independent from hard- and software.
- Laboratory Data Model (LAB)
- Case Report Tabulation Data Definition Specification (CRT-DDS)
- Also referred to as "define.xml", a machine readable version of the regulatory submission "define.pdf".
- Clinical Data Acquisition Standards Harmonization (CDASH)
- Defines a minimal data collection set for sixteen safety SDTM Domains, harmonizing element names, definitions and metadata. The objective is to establish a standardized data collection baseline across all submissions.
- CDISC Terminology
- Defines controlled terminology for SDTM and CDASH, provides extensible lists of controlled terms designed to harmonize data collected across submissions.
CDISC registered solutions providers
CDISC maintains a list of solutions providers, subject matter experts and consultants deemed to have sufficient knowledge and experience implementing the various CDISC standards.CDSIC registered solutions providers
ODM and EDC integration
Electronic Data Capture (EDC) systems can be certified as compliant with the Operational Data Model (ODM) by CDISC. There are two main types of integration, ODM Import and ODM Export.ODM Import
Full import allows importing of ODM-formatted clinical data (MetaData and Data).MetaData only import allows only the importing of MetaData. This is useful for setting up the EDC system to capture data. Basically allows third party software to define the forms, variables etc. used in the EDC system. This provides a EDC vendor-neutral system for defining a study.
See also
- Electronic Common Technical Document (eCTD)ECTDThe electronic Common Technical Document is an interface for the pharmaceutical industry to agency transfer of regulatory information.The content is based on the Common Technical Document format....
- Electronic Data CaptureElectronic Data CaptureAn Electronic Data Capture system is a computerized system designedfor the collection of clinical data in electronic format for use mainly in human clinical trials.Typically, EDC systems provide:* a graphical user interface component for data entry...
- Clinical data acquisitionClinical data acquisitionAcquisition or collection of clinical trial data can be achieved through various methods that may include, but are not limited to, any of the following: paper or electronic medical records, paper forms completed at a site, interactive voice response systems, local electronic data capture systems,...
- Clinical Data Management SystemClinical data management systemA clinical data management system or CDMS is a tool used in clinical research to manage the data of a clinical trial. The clinical trial data gathered at the investigator site in the case report form are stored in the CDMS...
(CDMS) - Data modelData modelA data model in software engineering is an abstract model, that documents and organizes the business data for communication between team members and is used as a plan for developing applications, specifically how data is stored and accessed....
- Data warehouseData warehouseIn computing, a data warehouse is a database used for reporting and analysis. The data stored in the warehouse is uploaded from the operational systems. The data may pass through an operational data store for additional operations before it is used in the DW for reporting.A data warehouse...
- Health Level 7Health Level 7Health Level Seven , is an all-volunteer, non-profit organization involved in development of international healthcare informatics interoperability standards...
- Health Informatics Service Architecture (HISA)
- LOINCLOINCLogical Observation Identifiers Names and Codes is a database and universal standard for identifying medical laboratory observations. It was developed and is maintained by the Regenstrief Institute, a US non-profit medical research organization, in 1994...
- SNOMEDSystematized Nomenclature of MedicineThe Systematized Nomenclature of Medicine is a multiaxial, hierarchical classification system . As in any such system, a disease may be located in a body organ which results in a code in a topography axis and may lead to morphological alterations represented by a morphology code.-Purpose:SNOMED...
- SNOMED CTSNOMED CTSNOMED CT , is a systematically organised computer processable collection of medical terminology covering most areas of clinical information such as diseases, findings, procedures, microorganisms, substances, etc...
- DICOMDigital Imaging and Communications in MedicineDICOM is a standard for handling, storing, printing, and transmitting information in medical imaging. It includes a file format definition and a network communications protocol. The communication protocol is an application protocol that uses TCP/IP to communicate between systems...
- Clinical trialClinical trialClinical trials are a set of procedures in medical research and drug development that are conducted to allow safety and efficacy data to be collected for health interventions...