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SAS 9.4 DISC Procedure: Users Guide SAS Documentation November 26, 2019The correct bibliographic citation for this manual is as follows: SAS Institute Inc. 2013. SAS 9.4 DISC Procedure: Users Guide.
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To fill out SAS 94 CDISC procedure, follow these steps:
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Ensure that you have the necessary data and documentation for the study.
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Familiarize yourself with the CDISC standards and guidelines for the study.
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Set up your SAS environment and ensure you have the necessary libraries and access to the required datasets.
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Identify the variables and data elements that need to be included in the CDISC submission.
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Use the SAS 94 CDISC procedure to transform and map the data to comply with the CDISC standards.
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Validate the transformed data to ensure accuracy and completeness.
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Generate the necessary CDISC submission files and documentation.
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Review the submission files and documentation for any errors or inconsistencies.
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Submit the CDISC dataset and documentation to the appropriate regulatory authority or sponsor.
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Keep track of any updates or changes to the CDISC standards and procedures for future studies.

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SAS 94 CDISC procedure is a set of standards for the submission of clinical data to regulatory authorities.
Biopharmaceutical companies conducting clinical trials are required to file SAS 94 CDISC procedure.
SAS 94 CDISC procedure can be filled out using specialized software that follows the CDISC standards.
The purpose of SAS 94 CDISC procedure is to ensure that clinical data submitted to regulatory authorities is in a standardized format for easier review.
SAS 94 CDISC procedure requires the reporting of clinical trial data including patient demographics, adverse events, and efficacy measures.
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