Product Overview
Streamline Data Management process with most advance, robust and secure ClinVigilant EDC (Electronic Data Capture) Platform. ClinVigilant EDC Platform is consisting of various modules, each designed to handle different aspects of clinical trial data management processes. These modules work together to provide a comprehensive solution for researchers and cross-functional and cross-study data insight.
Modules include:
- Study Design Module
- Data Entry and Collection Module
- Data Management and Query Module
- Safety Monitoring and Adverse Event Reporting Module
- Monitoring and Compliance Module
- Reporting and Analytics Module
- User Management and Security Module
- Integration and Interoperability Module
- Patient Management Module
- Study Administration Module
Deployment
- Web based
- Cloud Hosted
Pricing
- Subscription
- License Fee
More Information
Study Design Module
- Form Builder: Allows users to create and customize electronic case report forms (eCRFs) for data collection.
- Protocol Management: Tools to define and manage study protocols, including visit schedules, inclusion/exclusion criteria, and randomization procedures.
- Workflow: Design study specifications independent or complex workflow.
- Scheduling: Allows to set up schedule of visits that comes in sequential manner, visit interval along with positive and negative deviations.
Data Entry and Collection Module
- eCRF Completion: Interface for data entry, including features for entering patient data, lab results, and other relevant information.
- Data Validation Rules: Functions to check data for completeness and accuracy, with alerts for any discrepancies or missing information.
Data Management and Query Module
- Query Management: System for generating and managing queries to resolve data inconsistencies or missing data.
- Data Cleaning Tools: Tools to assist in data verification and cleaning to ensure high-quality data for analysis.
Safety Monitoring and Adverse Event Reporting Module
- Adverse Event Tracking: Features for recording and tracking adverse events and other safety data.
- Safety Reporting: Tools to facilitate the generation and submission of safety reports to regulatory authorities and ethics committees.
About the company
From decentralized trials to our clinical trial consulting services, our therapeutic, technical and functional team is underprop by the culture of ethics and patient safety. Our strong conviction and commitment is to our clients in bringing the next generation quality therapies faster to the market.
Our experts and developers can work on complex business challenges with your team to help you achieve your goals and define a roadmap of necessary changes, whether by implementing new solutions or transforming existing legacy processes