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ClinVigilant RTSM
Manage and track the randomization, treatment assignment, and data collection process.

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

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

Customization and Flxibility

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.
Patient-Centric Approach

Key Features of


Automated randomization of participants into different treatment groups or arms. This ensures unbiased assignment and reduces the risk of selection bias.

Treatment Allocation​

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.

Drug Supply Management

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.

Blinding and Masking​

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.

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.

Reporting and Analytics​​

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.

Security and Compliance​

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).

Remote Access and Mobile Compatibility

Provides remote access and mobile compatibility, allowing trial staff and participants to access the system from anywhere.

Security and Data Protection

Ensures the security of sensitive trial data with robust data protection measures and compliance with data privacy laws.

User Training and Support:

Includes comprehensive user training and support services to ensure effective use of the software.

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