
EDC
A customizable electronic data capture system for clinical trials, offering features like eConsent, ePRO, and advanced data management.
Overview
The electronic data capture (EDC) system is designed to meet the unique needs of clinical trial sites, providing end-to-end services that are user-friendly and efficient. It offers a comprehensive suite of features to ensure successful trial execution with just a few clicks.
EvidentIQ's EDC system is cost-effective, scalable, and compliant, utilizing advanced clinical trial software technologies to deliver high value while maintaining compliance and quality. The system includes flexible features such as DICOM image upload, image-based data entry, eConsent, ePRO/eDiaries accessible via various devices, RTSM modules, MedDRA and WHODrug coding, and advanced data extraction capabilities. It is customizable for a wide range of study types, including drug, medical device, diagnostic, observational, and more.
The system is accessible globally 24/7, offering consistent performance and flexible pricing models tailored to usage expectations. This ensures that users only pay for the features they need, with options for single or multiple study packages.
Key Features
- Fast Setup and Easy to Learn: The software allows for quick study setup and management, with customizable workflows that are simple to implement.
- Randomization and Supply Logistics: Integrated systems for managing medical device and drug logistics.
- Medical Coding: Supports MedDRA and WHODrug dictionaries for efficient coding of clinical data.
- CDISC Certified: Ensures interoperability and conformity with CDISC standards throughout the study lifecycle.
- Source Data Verification: Provides targeted verification processes to maintain data quality and integrity.
- eDiary & ePRO: Advanced web survey software for creating and managing patient questionnaires and forms.
- eCOA: Enhances data quality and protocol execution with user-friendly technology.
- Dashboards: Offers dynamic and static dashboards for study monitoring and data visualization.
- eConsent: Includes a compliant solution for digital and remote patient consenting.
- Designer Interface: Allows easy design of electronic forms without programming knowledge.
- Process Automation: Automates study events and reduces the need for in-person site visits.
- Open Architecture and Integration: Facilitates seamless integration with third-party applications and connected sensor technologies.
Overall, the EDC system is built with the end user's needs in mind, offering a flexible, accessible, and comprehensive solution for managing clinical trial data efficiently.


