Complete Guide to eISF +
Remote Site Access in Clinical Trials
How clinical operations leaders leverage remote site access technology to enable remote monitoring, start-up, management, and SDR/V.
You need remote access to your study sites, and you need your strategy to not fail. After working with over 10,000 study sites across 44 countries to implement eISF + Remote Site Access platforms, we know the secrets to how Sponsors/CROs can enable true remote site access, monitoring, and SDV/R at their study sites.
This guide will show you best practices, how-tos, and insights for implementing your own remote site access strategy: what is the eISF and how does it enable remote site access, how you can select a platform that will work for you and your sites, how to maximize the benefits, and how to get your study sites on board.
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“Florence’s [eISF + Remote Site Access] platform is helping us to respond to the changing environment due to COVID-19 and further progress COVID-19 research with the capability to perform remote monitoring where approved by regulatory authorities and ethics committees.”
Rob Goodwin
Vice President and Head of the Operations Center of Excellence in Global Product Development
Pfizer
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Brought to you by the eISF + Remote Site Access Experts
Key Benefits of eISF + Remote Site Access