ClinicalPURSUIT
About ClinicalPURSUIT
ClinicalPURSUIT is a clinical data management software from Global Vision Technologies designed for clinical research organizations. It provides data collection, monitoring, and reporting features so users can manage clinical trials effectively. The platform supports real-time data access, electronic data capture, and compliance tracking. ClinicalPURSUIT is designed to help researchers ensure data integrity and simplify the trial process. The solution is tailored for various clinical environments, including drug development and medical device trials. Key capabilities: data collection compliance tracking electronic data capture real-time monitoring reporting tools Best for: clinical researchers and trial managers that need to manage and analyze clinical trial data efficiently.
ClinicalPURSUIT by Global Vision Technologies is an Electronic Data Capture (EDC) system designed to enhance clinical trial data management. It provides essential functionalities such as study design tools, workflow management, real-time reporting, and regulatory compliance with standards like 21 CFR Part 11. The system aims to streamline data collection and improve efficiency, ensuring that clinical research teams can manage studies effectively while maintaining high data integrity. Although specific details about its interface are not publicly available, modern EDC platforms typically offer a web-based, user-friendly experience with customizable forms, automated edit checks, and role-based access controls to enhance usability. Functionally, ClinicalPURSUIT focuses on core clinical trial needs, including patient data collection, data validation, cleaning, and reporting. It is built to manage large volumes of clinical trial data while maintaining security and regulatory compliance. The platform is expected to support integration with other essential systems like Clinical Trial Management Systems (CTMS) and electronic Patient-Reported Outcomes (ePRO) tools, ensuring seamless data flow across various research processes.
Pros & Cons
- +• Improved Data Quality: Intelligent EDC and source data verification minimize errors, leading to cleaner data.
- +• Increased Efficiency: Automated workflows and rapid study development save time and resources.
- +• Reduced Costs: Streamlined processes and less manual intervention lower overall study costs.
- +• Enhanced Security: Advanced security measures protect sensitive data.
- +• Regulatory Compliance: Adherence to GCP, 21 CFR Part 11, and other regulations ensures compliance.
- +• Better Audit Trails: Granular auditing provides detailed tracking of all data changes and user activity.
- +• User-Friendly Design: Intuitive CRFs and powerful tools simplify study management.
- −• Dependence on Vendor: Reliance on a single vendor for EDC and registry solutions can create potential challenges if issues arise.
- −• Limited Information Available: The provided text focuses on features; details on pricing, specific integrations, and in-depth comparisons with competitors are missing. More research would be needed to fully assess these aspects.
- −• No Mention of Specific Integrations: The documentation doesn't mention if it integrates with other clinical trial management systems. This could be a limitation if integration is required.
Features
Key features
- • Intelligent Electronic Data Capture (EDC)
- The system uses smart logic to identify potential data errors before they enter the database, improving data quality.
- • Usable Clinical Report Forms (CRFs)
- CRFs are designed intuitively to minimize user errors during data capture.
Additional features
- • Source Data Verification
- Data is checked for errors at the point of entry, ensuring accuracy from the start.
- • Advanced Data Security
- Robust security measures protect collected data.
- • Cost Reduction
- Configurable data capture and workflows automate processes, reducing costs and labor.
- • Regulatory Compliance
- The system complies with GCP, 21 CFR Part 11, and other relevant regulations.
- • Advanced Real-time Auditing
- Granular auditing tracks all user activity and data entry, allowing for detailed review of changes.
- • Rapid Study Development
- Tools are designed for quick study setup and execution.
- • Powerful Data Management Tools
- The platform provides robust tools to streamline study management.
Pricing
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About ClinicalPURSUIT
ClinicalPURSUIT is a clinical data management software from Global Vision Technologies designed for clinical research organizations. It provides data collection, monitoring, and reporting features so users can manage clinical trials effectively. The platform supports real-time data access, electronic data capture, and compliance tracking. ClinicalPURSUIT is designed to help researchers ensure data integrity and simplify the trial process. The solution is tailored for various clinical environments, including drug development and medical device trials. Key capabilities: data collection compliance tracking electronic data capture real-time monitoring reporting tools Best for: clinical researchers and trial managers that need to manage and analyze clinical trial data efficiently.
ClinicalPURSUIT Details
ClinicalPURSUIT's In-App Market Place
Does ClinicalPURSUIT have an in-app market place?
Yes
How many Mini-Apps in the marketplace?
1
Mini Apps
N/A
Pricing Options
Accepted Payment Currencies
USD ($), EUR (€), GBP (£), JPY (¥), AUD (A$), CAD (C$), CHF (CHF), CNY (¥), SEK (kr), INR (₹), SGD (S$), HKD (HK$), NOK (kr), KRW (₩), NZD (NZ$), MXN (Mex$), BRL (R$), RUB (₽), ZAR (R)
Pros & Cons
- • Improved Data Quality: Intelligent EDC and source data verification minimize errors, leading to cleaner data.
- • Increased Efficiency: Automated workflows and rapid study development save time and resources.
- • Reduced Costs: Streamlined processes and less manual intervention lower overall study costs.
- • Enhanced Security: Advanced security measures protect sensitive data.
- • Regulatory Compliance: Adherence to GCP, 21 CFR Part 11, and other regulations ensures compliance.
- • Better Audit Trails: Granular auditing provides detailed tracking of all data changes and user activity.
- • User-Friendly Design: Intuitive CRFs and powerful tools simplify study management.
- • Dependence on Vendor: Reliance on a single vendor for EDC and registry solutions can create potential challenges if issues arise.
- • Limited Information Available: The provided text focuses on features; details on pricing, specific integrations, and in-depth comparisons with competitors are missing. More research would be needed to fully assess these aspects.
- • No Mention of Specific Integrations: The documentation doesn't mention if it integrates with other clinical trial management systems. This could be a limitation if integration is required.
ClinicalPURSUIT's Support Options
Contact
877-791-4367ClinicalPURSUIT's Alternatives
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