Trial Data Captured Digitally, Validated Instantly

eClinical Data Capture System for Accurate, Efficient Trial Data

Use our E-Clinical Data Capture System for digital recording, validation, and management of clinical trial data to ensure that every clinical trial site and data management team gets a quick, efficient, and totally compliant electronic data capture system providing quality data from the first patient encounter to database lock.

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Clinical Trial Management

Why Use Our System?

Replace Paper Data Collection with a Smarter eClinical Environment

ECDCS delivers the clinical research team a complete electronic data capture solution, validated and compliant with regulatory guidelines, replacing the traditional paper case report form with an intelligent electronic form that benefits from real-time data validation and automated query generation. Regardless of whether we talk about a complex design of a study involving several visits or adaptive trial data model or patient-reported outcomes, all data collection scenarios are covered by ECDCS.

Give every trial site a faster, more accurate way to capture patient data that reduces errors, cuts query volumes, and accelerates the path to a clean, locked database.

See System Documentation

Intelligent eCRF Design

Configurable Electronic Case Report Forms for Every Study Design

Dynamic, rule-driven eCRFs that adapt to each patient’s data and guide site staff through every data entry requirement. Form design flexibility that accommodates even the most complex protocol structures without sacrificing data quality.

The system offers an extensive no-code design tool for creating dynamic forms with embedded rules that can validate the data input at the same time. This feature allows you to save time on reviewing queries after the data collection stage since you can eliminate potential errors while entering information into the electronic case report forms.

Explore eCRF Design Tools
Clinical Trial Management
Clinical Trial Management

System Integration

Connected to Your CTMS, Safety, and Regulatory Platforms

Data captured in the system flows automatically to every connected research platform. Integration that eliminates manual data transfers and keeps every system in your research ecosystem synchronized.

Using CDISC CDASH and HL7 FHIR, the system interoperates with best-of-breed CTMS solutions, pharmacovigilance systems, central laboratory systems, randomization and supply management systems, and electronic submission environments. Complete application programming interfaces (APIs), detailed integration guides, and implementation assistance guarantee quick and seamless integration into any clinical research technology architecture.

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Data Quality and Lock Efficiency

Clean Data, Faster Database Lock, Stronger Submissions

Fewer queries, faster resolution, earlier database lock. Data quality built in from the first entry that accelerates every milestone from data freeze to regulatory submission.

The real-time validation, automated detection of inconsistencies, creation of electronic audit trails, and compliance with electronic signatures as per 21 CFR Part 11 guidelines guarantees that each data record captured is in accordance with the regulations regarding the quality, accuracy, and traceability of the data record in question.

Learn About Data Quality Outcomes
Clinical Trial Management

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