The Clinical Data Interchange Standards Consortium Laboratory Model: Standardizing Laboratory Data Interchange in Clinical Trials

The Laboratory Data Standards Model team of the Clinical Data Interchange Standards Consortium (CDISC) has defined a model for representing, in a standardized manner, the laboratory data generated during the conduct of clinical trials. The CDISC Laboratory Data Standards Model is the first step in p...

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Published inDrug information journal Vol. 37; no. 3; pp. 271 - 281
Main Author Bassion, Susan
Format Journal Article
LanguageEnglish
Published Los Angeles, CA SAGE Publications 01.01.2003
Springer Nature B.V
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Abstract The Laboratory Data Standards Model team of the Clinical Data Interchange Standards Consortium (CDISC) has defined a model for representing, in a standardized manner, the laboratory data generated during the conduct of clinical trials. The CDISC Laboratory Data Standards Model is the first step in proposing independent standards for the interchange of clinical trial laboratory data. Standards will decrease the time and resources that are required to exchange data by stakeholders in the pharmaceutical development process. Cost containment and improved data quality should result from the adoption of such a standard for interchanging laboratory data.
AbstractList The Laboratory Data Standards Model team of the Clinical Data Interchange Standards Consortium (CDISC) has defined a model for representing, in a standardized manner; the laboratory data generated during the conduct of clinical trials. The CDISC laboratory Data Standards Model is the first step in proposing independent standards for the interchange of clinical trial laboratory data. Standards will decrease the time and resources that are required to exchange data by stakeholders in the pharmaceutical development process. Cost containment and improved data quality should result from the adoption of such a standard for interchanging laboratory data.
The Laboratory Data Standards Model team of the Clinical Data Interchange Standards Consortium (CDISC) has defined a model for representing, in a standardized manner, the laboratory data generated during the conduct of clinical trials. The CDISC Laboratory Data Standards Model is the first step in proposing independent standards for the interchange of clinical trial laboratory data. Standards will decrease the time and resources that are required to exchange data by stakeholders in the pharmaceutical development process. Cost containment and improved data quality should result from the adoption of such a standard for interchanging laboratory data.
Author Bassion, Susan
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  article-title: A multidisciplinary approach to data standards for clinical development—progress update
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SubjectTerms Clinical data
Clinical Data Interchange Standards Consortium
Clinical trials
Computerized records management
Consortia
Containment
Data exchange
Exchanging
Laboratories
Medical records
Title The Clinical Data Interchange Standards Consortium Laboratory Model: Standardizing Laboratory Data Interchange in Clinical Trials
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