Enhance data accuracy, compliance, and efficiency with our secure EDR system for clinical trials.

Features of the EDR System

 
01

Data Collection & Integration

Seamlessly collect and integrate clinical trial data from multiple sources, including EDC, ePRO, and wearable devices, ensuring real-time accuracy and compliance.

02

User-Friendly Interface

Our intuitive UI design enables researchers, CROs, and sponsors to navigate, input, and monitor clinical data effortlessly, reducing errors and improving efficiency.
03

Security & Compliance

Ensuring data integrity with encryption, audit trails, and compliance with FDA 21 CFR Part 11, HIPAA, and GDPR, safeguarding patient confidentiality.

04

Continuous Support & Optimization

Dedicated 24/7 support, training, and regular system updates to keep your EDR system running smoothly, adapting to evolving regulatory standards.

Streamlining Clinical Trials with Advanced Electronic Data Records

EDRS, or Electronic Data Record System, is a tool used for managing clinical trial information. It is the central system used for collecting, storing, and organizing data as it comes in, like a paper-based system. EDRS supports the recording and tracking of all trial data across the lifecycle and helps ensure accuracy, regulatory compliance, and consistency. Functionality like automated data input, audit trails, and secure access controls mitigate error risk while ensuring data integrity. These systems even support real-time tracking and remote monitoring, enabling sponsors and stakeholders to effectively monitor trial progress.Oldest in Clinical Trials: EDRS greatly improves for the clinical trials. EDRS also integrates with other systems such as EHRs and CTMS, effectively eliminating redundancy in processes and facilitating a seamless data workflow.