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Pharmacy China 2016 Paper 24Building Your Own DISC Application with SAS Clinical Standards Toolkit Jing GAO, SAS R&D, Beijing, China ABSTRACT The SAS Clinical Standards Toolkit (CST) is a framework
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Building your own CDISC (Clinical Data Interchange Standards Consortium) refers to creating datasets in compliance with CDISC standards for clinical trials.
Clinical researchers, pharmaceutical companies, and other organizations conducting clinical trials are required to file building their own CDISC datasets.
CDISC datasets can be filled out by using CDISC-compliant software tools for data collection, transformation, and submission.
The purpose of building your own CDISC is to ensure that clinical trial data is collected, stored, and reported in a consistent and standardized format for regulatory submissions.
Building your own CDISC datasets must include key information such as study protocol, subject demographics, adverse events, and clinical outcomes.
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