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Visualizing and Validating Metadata Traceability within the CDISC Standards
The Food & Drug Administration has begun requiring that electronic submissions of regulated clinical studies utilize the Clinical Data Information Standards Consortium data standards. Within regulated clinical research, traceability is a requirement and indicates that the analysis results can be...
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| Gepubliceerd in: | AMIA Jt Summits Transl Sci Proc |
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| Hoofdauteurs: | , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
American Medical Informatics Association
2017
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5543378/ https://ncbi.nlm.nih.gov/pubmed/28815125 |
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