Product Overview
Configurable Role-Based CTMS. Enhance productivity and collaboration for research teams by efficiently managing regulatory workflows. Organize all site documentation and study data in one centralized location. Use robust reporting and analytics tools to help you ensure important milestones are met.
- Increases visibility by removing data silos
- Provides transparency and drives collaboration
- Fully configurable to optimize processes
- Generates site visit documents
- Easy monitoring of study progress and performance
Deployment
- Web based
- Cloud Hosted
Pricing
- Subscription
- License Fee
More Information
Features
- Investigator database with site creation and contact management
- Site visit scheduling and management
- On-site/remote monitoring visit documentation with eSignature and eTMF integration
- Protocol deviation, action item, and communication log management
About the company
At Remarque Systems, our mission is simple: provide a single, easy, and effective platform to manage all your clinical trial data. We deliver this through an intuitive and flexible platform that:
Consolidates all your data from different sources in real-time
Delivers end-to-end visibility and oversight with data-driven analysis, monitoring, and risk assessment
Drives better-informed decisions with clear and conclusive analytics, reports, and visualizations
The result: Consolidating your data on one powerful platform brings process optimization, increased visibility, rapid communications, and improved quality to your clinical trials.