As precision medicine and immunotherapies are becoming the forefront of clinical trials, sites are tasked with triple the workload without triple the resources. Purpose-built eSource and regulatory tools allow centers to scale and optimize document management, provide oversight and increased visibility for project management, ensure compliance, and become the central hub of all trial tasks from startup to closeout. We discovered that return on investment spanned seven areas, specifically , resulting in a positive economic impact of nearly $20,000 per study.
Conclusion
Custom ROI Analysis Our team can provide you with a custom ROI analysis for your site, CRO, or Sponsor based off your unique situation.
Email us at info@florencehc.com to learn more and discover Florence eBinders™
The ROI of an eRegulatory Platform
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