Electronic Data Capture in Clinical Trials

Accelerate Study Build & Database Lock

CDP’s AI-enhanced EDC puts a world of data in the palm of your hand.

You can now leverage the industry’s first AI-enhanced eCRFs along with our Zero Data Entry™ solution via FHIR and EHR. Our highly evolved data collection system has been refined and optimized over an impressive 15-year legacy. Large or small, simple or complex, we have the tools and knowledge to help you accomplish your most demanding data capture objectives.

AI-Powered text analytics allows you to extract and classify clinical trial data from unstructured medical texts with improved efficiency and accuracy. This integrated functionality allows you to identify relevant keywords and phrases, infer meaningful connections, compile statistics, and streamline data analysis.
Our Zero Data Entry™ solution using FHIR (Fast Healthcare Interoperability Resources) and Universal Data Integration Gateway (UDIG) with EHR (Electronic Health Records), and RWD (Real World Data) improves data quality and speeds collection, while removing the burden of arduous, tedious entry of subject data already contained in EHRs. Only Simplified Clinical offers ZDE™ technology to optimize the efficiency and accuracy of your data collection.
Collect data from wearable, portable devices via standardized IoT connections.
Take advantage of faster study builds with reusable eCRF libraries that include complete forms, fields, and edit checks while enabling/supporting enterprise data standardization.

Access RWD sources, public and private wherever they reside, all in accordance with applicable regulatory and privacy laws.
Accelerate data entry and cleaning with adaptive eCRFs, online data clarification and query resolution.
Facilitate rapid system adoption with intuitive web-based training, providing all CDP users with the knowledge they need to utilize our platform efficiently, cost-effectively and in compliance with all regulatory requirements.
Improve and simplify the user experience with a single user login that provides access to all authorized studies and platform functions.
Assure accurate, up-to-the-minute data collection specifications with mid- study protocol changes implemented in real time without interruption.
“Quick-lock” your study data once it has been cleaned, reviewed, and approved. With the click of a button your database is locked, allowing analysis to commence sooner and regulatory submission to occur without delay.

Electronic Data Capture with Our Zero Data Entry™ Capture Solution

Accelerate Study Build & Database Lock

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