Clinical Safety Reporting
Deploy and Track Safety Letters Across Studies
Simply and effectively distribute safety reports to clinical investigators across all studies and programs utilizing a specific investigational drug.
Effective and Compliant Safety Report Distribution
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Mobile-optimized, Part 11-compliant eSignatures
Each investigator can confirm receipt on their mobile, desktop, or tablet using their 21 CFR Part 11 eSignature.
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Shared signatures across multiple studies
Submissions and signatures are shared across all relevant studies, requiring only one report submission for a multi-study program, and one signature from the investigator.
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Audit trail and real-time reports
Signatures are time and date stamped to ensure a full audit trail and sponsors can run real-time reports showing the status and response rate. The Longboat Platform’s virtual dashboards allow sponsors to quickly drill down to regions and sites where there has not yet been a response.
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Intuitive, familiar interface
Sites and sponsors already working within the Longboat Platform can action their reports in a familiar environment already used for multiple study tasks like training, visit implementation, pre-screening, and more.
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Distribute reports worldwide
Deployed in over 60 countries, Longboat’s safety reporting provides a global solution to deployment, tracking, and reporting of safety reports.
