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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

Vendor
Global Vision Technologies
Year Launched
2011
Location
222 South Central Ave Clayton, MO 63117
Deployment
cloud
Training Options
documentation, videos, live online, in person
Countries Served
All Countries
Languages
English
Users
Clinical Research Coordinators, Data Managers, Principal Investigators, Statisticians
Industries Served
Healthcare, Pharmaceutical, Biotechnology, Research
Tags
Clinical Trial Management, Electronic Data Capture, Clinical Research, Data Management, Health Sciences, Research Study, Clinical Trials, Patient Enrollment, Regulatory Compliance, Electronic Case Report Form, Data Validation, Remote Monitoring, Study Protocol, Investigator Site, Clinical Data Management.

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

Free trial
Free version
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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.

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