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DISC Protocol Controlled Terminology, 20180330
Sources: NCI EVS Terminology Resources website: http://www.cancer.gov/cancertopics/cancerlibrary/terminologyresources/cdisc
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How to fill out cdisc controlled terminology initiative
How to fill out cdisc controlled terminology initiative
01
Access the CDISC website and navigate to the Controlled Terminology page.
02
Review the list of terms available and determine which ones are relevant to your study.
03
Download the relevant terminology files in the appropriate format (e.g. Excel, XML).
04
Fill out the necessary fields with the requested information for each term.
05
Save the completed terminology file and upload it to the appropriate location as instructed by CDISC.
Who needs cdisc controlled terminology initiative?
01
Researchers conducting clinical trials who need to ensure consistent and standardized data collection and reporting.
02
Regulatory agencies who require standardized data formats for submissions and review.
03
Pharmaceutical companies looking to streamline their data management processes and improve data quality.
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What is cdisc controlled terminology initiative?
The CDISC Controlled Terminology Initiative is a project aimed at standardizing the terms used in clinical trials to ensure consistency and interoperability.
Who is required to file cdisc controlled terminology initiative?
All organizations conducting clinical trials are required to use CDISC controlled terminology for data submission to regulatory agencies.
How to fill out cdisc controlled terminology initiative?
CDISC controlled terminology can be filled out using standardized formats provided by CDISC, such as datasets, data standards, and coding tools.
What is the purpose of cdisc controlled terminology initiative?
The purpose of CDISC controlled terminology initiative is to improve the quality, efficiency, and interoperability of clinical trial data.
What information must be reported on cdisc controlled terminology initiative?
CDISC controlled terminology initiative requires reporting of standardized terms, definitions, and formats for clinical trial data.
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