SERVICES
RANDOMIZATION & CLINICAL TRIAL MANAGEMENT SOFTWARE
Optimized randomization (IRT) and trial supply management (RTSM) processes to automate your study design
The Power of Clinical StudyPal IRT
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- Randomization Methods: Clinical StudyPal IRT supports various randomization methods, including simple randomization, block randomization, and permuted block randomization. These options ensure that the trial design meets the specific needs of each study, maintaining the integrity of the randomization process.
- Stratification Options: Our software provides flexible stratification options, including blinded or unblinded settings. This flexibility allows for the customization of the randomization process according to the trial’s requirements.
Enrollment and Eligibility Forms: The setup of enrollment and eligibility forms with validation checks ensures that only eligible patients are randomized, maintaining the quality and reliability of the trial data.
Inclusion and Exclusion Criteria: The configuration of inclusion and exclusion criteria within the software helps automate patient selection, ensuring that the right patients are enrolled in the study.
Automated Notifications: Automatic email notifications are sent when a patient is randomized, keeping all stakeholders informed and ensuring smooth communication throughout the trial.
Patient Management: The software includes robust patient management and status tracking features, enabling real-time monitoring of patient enrollment and randomization status.
Enhancing Clinical Trial Supply Management
Efficient supply management is critical to the success of clinical trials. Clinical StudyPal IRT includes a comprehensive supply management module that ensures the right drug or device is received by patients on time and at the correct dosage.
Supply
Optimization
Our clinical study software utilizes resupply algorithms and automated supply management to optimize drug/device allocation, reducing costs and ensuring efficient use of resources.
Real-Time Management
Real-time dispensation management and supply status tracking provide up-to-date information, allowing for immediate adjustments and interventions when necessary.
Integration with Systems
Clinical StudyPal IRT integrates seamlessly with depot, EDC (Electronic Data Capture), and EMR (Electronic Medical Records) systems, ensuring a streamlined flow of information and enhancing overall trial efficiency.
Emergency
Unblinding
In case of emergencies, the software allows for real-time enrollment tracking and emergency unblinding, ensuring patient safety and compliance with regulatory requirements.
Key Benefits of Clinical Trial Randomization
Clinical trial IRT offers significant benefits to all stakeholders involved in clinical trials, including patients, sites, and sponsors.
For Patients:
Accurate Drug Dispensation: Ensures that patients receive the correct drug in the right dosage, enhancing treatment efficacy and compliance.
Compliance Monitoring: Drug accountability features assist in monitoring patient compliance, ensuring adherence to the treatment regimen.
For Sites:
Activation Control: The software provides site activation control, ensuring that sites are ready and compliant before starting the trial.
Dispensation Management: Real-time management of drug dispensation ensures that patients receive their treatments on schedule.
Supply Status Tracking: Real-time tracking of supply status helps manage inventory effectively and avoid stockouts.
For Sponsors:
Site Oversight: Sponsors can maintain oversight of sites, ensuring compliance and monitoring trial progress.
Batch Releases: The software supports batch releases, ensuring that drugs/devices are dispensed in a controlled and compliant manner.
Emergency Unblinding: Provides the ability to unblind in emergencies, ensuring patient safety and compliance with regulatory requirements.
LET'S TALK
Advanced Features for Enhanced Clinical Trial Supply Management
Clinical StudyPal IRT offers several advanced features that further enhance the management of clinical trials.
- Oversight Dashboards: The software includes oversight dashboards that provide a comprehensive view of the trial’s progress, enabling informed decision-making.
- Data Querying Capabilities: Advanced data querying capabilities allow for in-depth analysis of trial data, helping identify trends and areas for improvement.
- Interactive Reports: Interactive reports and on-demand data export features provide stakeholders with real-time insights into the trial’s progress and outcomes.
The Value of Clinical Trial Management Software
Implementing robust clinical trial management software like Clinical StudyPal IRT offers numerous benefits:
- Enhanced Efficiency: Automation of routine tasks and efficient management of trial logistics lead to faster and more efficient trial operations.
- Cost Reduction: Optimized supply management and reduced administrative burden result in significant cost savings.
- Improved Compliance: Real-time tracking and automated notifications ensure that trials comply with regulatory requirements and maintain high standards of quality.
- Better Patient Outcomes: Accurate drug dispensation and compliance monitoring lead to better patient outcomes, enhancing the overall success of the trial.
Why Choose Delve Health For Randomized Clinical Trial IRT?
Expertise in Clinical Trials
Our team of experts understands the complexities of clinical trial IRT and provides tailored solutions to meet your specific needs.
Comprehensive Support
We offer end-to-end support, from patient recruitment and randomization to supply management and compliance monitoring.
Advanced Technology Integration
Our Clinical StudyPal platform integrates advanced technology to enhance efficiency and streamline trial operations.
Global
Reach
With a global network of partners and resources, we ensure that your trial is supported effectively, regardless of location.
Frequently Asked Questions
Clinical StudyPal IRT optimizes clinical trial management by automating routine tasks, providing real-time data and analytics, and ensuring seamless integration with other systems. This leads to more efficient trial operations and better outcomes.
Clinical StudyPal IRT supports simple randomization, block randomization, and permuted block randomization. These methods help maintain the integrity of the randomization process, ensuring unbiased and reliable trial results.
The best clinical trial management systems include automated reminders for medication schedules and appointments, real-time tracking of patient status, and compliance monitoring tools that help ensure patients adhere to the trial protocols.
Yes, Clinical StudyPal IRT integrates seamlessly with depot, EDC (Electronic Data Capture), and EMR (Electronic Medical Records) systems. This integration ensures a streamlined flow of information and enhances overall trial efficiency.
Automated supply management reduces costs through optimized resupply algorithms, ensures timely delivery of drugs/devices, tracks expiration dates, and manages inventory effectively. This leads to smoother trial operations and better resource utilization.
Delve Health adheres to strict data protection regulations and implements robust security measures to safeguard patient and trial data. Our software ensures that all information is handled with the highest level of confidentiality and integrity.
Stratification in clinical trials involves grouping patients based on certain characteristics to ensure balanced and unbiased randomization. Clinical StudyPal IRT offers flexible stratification options, including blinded and unblinded settings, to meet the specific needs of each trial.
In case of emergencies, the best clinical trial management systems provide real-time enrollment tracking and the ability to unblind patients, ensuring their safety and compliance with regulatory requirements.
Delve Health offers comprehensive support for trial sites, including site activation control, real-time dispensation management, supply status tracking, and site oversight tools. This ensures that sites operate efficiently and comply with trial protocols.
