How Pharma and Trial Sites Can Rethink Communication
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Learn how electronic Investigator-Controlled Site File (eISF) can reduce cost, risk, and disruptive investigator visits.
Consider the limitations of a paper-based clinical trial document management system:
- On-site monitor visits are inefficient and costly, averaging $5,000 per day, per monitor
- Paper-based ISF systems contribute heavily to general failings
- As trial complexity increases, the costs and risks of relying on a paper-based site file system increase
"Today, 80% of site-based documentation is still fully paper based, with serious consequences for the entire clinical trial process."
Our new eBook, Secure File Sharing in a Disaggregated Industry: How Pharma and Trial Sites Can Rethink Communication, published in cooperation with industry-leading publisher FierceMarket, shows how an electronic Investigator-Controlled Site File (eISF) system can reduce cost, risk, and disruptive investigator visits by enabling secure remote monitoring.
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