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Coding analytics dashboard

The Coding Analytics dashboard of EDC provides insights into how data has been coded in the CODING app and identifies patterns that can impact the trial's reliability, such as adverse events occurring with subjects or interventional products used by subjects. This dashboard helps in monitoring coding discrepancies, assessing risk levels, and ensuring compliance with regulatory standards.

Important

To review data on the Coding Analytics dashboard, the following preconditions must be met:

In this section, you can learn how to perform actions discussed in the following sections:

In this section:

An eClinical application that is intended for medical coding and managing elements of data collected during clinical trials to organize large amounts of information in a standardized way—according to WHODrug and MedDRA dictionaries. The application facilitates data analysis and ensures accuracy and consistency in reporting.

Get to know all the possibilities of the app with the comprehensive CODING User Guide.

Any untoward medical occurrence in a clinical investigation subject administered a pharmaceutical product that does not necessarily have a causal relationship with this treatment. An adverse event (AE) can therefore be any unintended sign (including an abnormal laboratory finding), symptom, or disease temporally associated with the use of a medicinal (investigational) product, whether or not related to the medicinal (investigational) product.

An eClinical application that provides functionality to design and configure a study (clinical trial), namely to configure CRFs, set subject phases, visits, and others.

The application supports the design of the CDSIC ODM-compliant electronic CRFs to support EDC and eDiary data collection and management.

Get to know all the possibilities of the app with the comprehensive SD User Guide.