Product Overview
ClinVigilant RTSM © streamlines the management of clinical trials, improves efficiency, reduces errors, and enhances data quality. It enables researchers to effectively monitor and manage the entire study process, ensuring accurate and reliable results.
What Makes ClinVigilant RTSM different from other solution provider?
Integration and Compatibility
Clinvigilant RTSM seamlessly integrates with various other clinical trial systems, such as electronic data capture (EDC) systems, electronic patient-reported outcome (ePRO) platforms, and drug supply management systems. This integration streamlines data flow and eliminates manual data entry errors, enhancing overall trial efficiency and accuracy.
Real-time Monitoring
Clinvigilant RTSM provides real-time monitoring of clinical trial data. This allows researchers and sponsors to have immediate access to important information, enabling them to make quick and informed decisions. Real-time monitoring also helps identify any potential issues or anomalies early on, improving the overall efficiency and safety of the clinical trial.
Customization and Flexibility
Clinvigilant RTSM offers a high level of customization and flexibility. It allows researchers to tailor the system according to their specific requirements, study protocols, and therapeutic areas. This adaptability ensures that the solution is well-suited to the unique needs of each clinical trial.
Patient-Centric Approach
Clinvigilant RTSM places a strong emphasis on patient-centricity. It provides user-friendly interfaces for patients to easily report trial data and engage with the system. By prioritizing patient convenience and adherence, Clinvigilant RTSM improves patient compliance and reduces data collection challenges.
Deployment
- Web based
- Cloud Hosted
Pricing
- Subscription
- License Fee
More Information
Automated randomization of participants into different treatment groups or arms. This ensures unbiased assignment and reduces the risk of selection bias.
Manages the allocation of treatments to participants based on the randomization process. It ensures that the appropriate treatment and Kit is assigned to each participant according to the study protocol.
Tracks the availability of investigational drugs and manages the supply chain at either local depot or central. It helps in ensuring proper drug distribution, managing inventory, and preventing stockouts.
Supports blinding and masking procedures by securely storing information regarding treatment allocations. This helps maintain the integrity of the study by preventing bias in treatment administration and data collection.
Facilitates real-time data collection by allowing researchers to enter and access study data electronically. It enhances data accuracy and reduces the chance of human error associated with manual data entry.
Generates various reports and analytics to provide insights into the study progress and treatment efficacy. It helps researchers monitor and evaluate the study outcomes effectively.
Maintain strict security measures to protect sensitive patient information and ensures compliance with regulatory guidelines, such as GDPR, HIPAA (Health Insurance Portability and Accountability Act) and GCP (Good Clinical Practices).
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