CDISC

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CDISC

Clinical Data Interchange Standards Consortium. A global, open, multidisciplinary, non-profit organisation that has established standards to support the acquisition, exchange, submission and archive of clinical research data and metadata. The CDISC mission is to develop and support global, platform-independent data standards that enable information system interoperability to improve medical research and related areas of healthcare.  CDISC standards are vendor-neutral, platform-independent and freely available.
References in periodicals archive ?
CDISC, the Clinical Data Interchange Standards Consortium, is an open, multidisciplinary non-profit organization that has established worldwide industry standards to support the electronic acquisition, exchange, submission and archiving of clinical study data.
These include Medidata Developer Central, an online community that supports developers' efforts to integrate clinical trial solutions with Medidata Rave, and Medidata Rave Web Services API, a Clinical Data Interchange Standards Consortium (CDISC)-compliant tool designed to facilitate rapid integrations with Medidata Rave for real-time data sharing using data standards.
Nextrials was nominated for its contribution to the industry, specifically through participation with industry organizations, such as the Clinical Data Interchange Standards Consortium (CDISC) and Integrating the Healthcare Enterprise (IHE), in developing and implementing EDC and EHR integration standards.
Accredited Standards Committee (ASC) X12,, ASTM International, and Clinical Data Interchange Standards Consortium (CDISC).
The WebSDM software supports the validation and review of clinical trials study data submitted by bio-pharmaceutical companies in the Study Data Tabulation Model (SDTM) format developed by the Clinical Data Interchange Standards Consortium (CDISC).
The Clinical Research Information eXchange (CRIX) International today announced their participation with Pfizer, Partners HealthCare and the Clinical Data Interchange Standards Consortium (CDISC) in the ASTER (Adverse Drug Event Spontaneous Triggered Electronic Reporting) study, which is exploring ways to improve the current spontaneous reporting system (SRS), the primary source of information for adverse drug events.
AUSTIN, Texas -- The Clinical Data Interchange Standards Consortium (CDISC) announced today an authoritative line up of keynote speakers and the promise of a robust information exchange forum at this year's CDISC International Interchange (26-31 October 2008).
AUSTIN, Texas -- The Clinical Data Interchange Standards Consortium (CDISC), announced today that the Food and Drug Administration (FDA) selected CDISC, via a formal RFP process, to provide training to FDA reviewers of regulatory submissions.

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