Cost Reduction from Streamlined Workflows
Workflows are the heart of clinical trial document management. Review and signature processes for 1572s, financial disclosure, protocols, and serious adverse events absorb research staff time as they manage compliance considerations like routing, form completion, annotation and signatures. Secondary tasks in these workflows create additional waste. Repeat filing of similar documents from study to study, scanning and printing documents between digital and physical states, maintaining paper logs and to-do lists, and printing and filing emails for correspondence binders all steal precious hours from coordinator to principal investigator. Pre-programed eBinder workflows can eliminate the administrative burden on investigators, minimize the likelihood of misplaced documents, drive consistency, and provide a new level of process oversight to clinical trial management. Documentation processes move faster and require less work, allowing teams to go faster while focusing on more important tasks.
$3,600 per study per year
Net: Electronic document routing editing and signatures removes an estimated person-day per month, per study— $300 per day each month equals approximately $3,600 a year per study.
The ROI of an eRegulatory Platform
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