The Only All-in-One platform for research sites.
Simple, efficient and compliant
100% Satisfactory FDA Inspections
Multi-study, Multi-site, Multi-language, Multi-currency & Multi-country
Reduces the start of study in 3 – 4 weeks with a quick and cost-effective execution.
Patient-centered
Easy to use, accessible from any browser, wherever and whenever
Automated Workflows
Integrate with EDC, IRT, eCRF and other systems if necessary
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Integra IT.
For Sites.
Other Solutions.
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