CONFORM™ EDC is a feature-rich data collection tool, fully integrated with the eClnical Suite, providing for seamless trial execution.
CONFORM™ EDC provides:
– Comprehensive CRF Design and Library Support
– Local Lab and External Data Management
– Extensive Reporting for Full Study Oversight
– Advanced SAE Reporting & Medical Coding
– Alerts & Notifications for Proactive Trial Management
– Full Life-Cycle Management
The CONFORM™ eDiary/ePRO/eCOA component is a comprehensive tool for managing patient-reported outcomes and other clinical assessments electronically. This module is an essential part of the CONFORM™ eClinical Platform, providing a seamless experience for both patients and clinical staff, ensuring high-quality data capture, and enhancing patient engagement.
Designed to streamline clinical trials, CONFORM™ eDiary/ePRO/eCOA enables the capture of patient-reported data and clinician assessments in real-time, offering a fully integrated, end-to-end solution that is interoperable with other CONFORM™ modules.
Capabilities include:
– Open Architecture for Easy Integration
– Robust eCOA Capabilities
– Enhanced Patient Engagement
– Real-Time Data Ingestion and Synchronization
– High Performance and Intuitive Interface
– Comprehensive Reporting and Analytics
EDETEK presents its deep domain expertise with advanced technologies such as AI/ML, advanced analytics, and integrated data pipeline to launch a next generation RQBM solution. This RBQM solution offers a comprehensive, real-time approach to managing trial quality and monitoring risks, from data integration to issue resolution.
With advanced analytics and seamless integration with EDETEK’s innovative technology, you can trust our CONFORM™ platform to deliver superior trial oversight.
The CONFORM™ RTSM (Randomization and Trial Supply Management) is an essential part of the CONFORM™ eClinical Platform, providing seamless randomization and trial supply management for clinical trials. As a part of an integrated, end-to-end solution, CONFORM™ RTSM ensures efficient handling of patient assignments, treatment allocation, and investigational product management—all from a single, intuitive platform.
Capabilities include:
– Support for Complex and Adaptive Study Designs
– Efficient Randomization and Supply Management
– Built-In Metrics and Comprehensive Reporting
– Support for Risk-Based Monitoring
– Remote Monitoring Support
– Accelerate Study Start-Up
