Complete Guide To eISF + Remote Site Access In Clinical Trials

Clinical trial sites are rapidly shifting to performing the bulk of their clinical trial operations on cloud-based systems.

This rapid shift to digital document and data management solutions, specifically the Electronic Investigator Site File (eISF), opens the door to innovative remote collaboration solutions to accelerate research and reduce operational costs.

The sponsor/CRO clinical operations leader has  a unique opportunity to take advantage of this rapid shift by integrating remote site access with the eISF.

This guide compiles Florence’s experience migrating over 7,200 study sites in 27 countries to our eISF + remote site access and collaboration platform that hosts over 2 million monitoring events per month.

In this guide you will find:

• An overview of eISF + Remote Site Access for remote site start-up, monitoring, and SDR/V
• The short-term and long-term impact of eISF + Remote Site Access
• How to make your remote site access and monitoring plan successful with sites
• The types of eISF + Remote Site Access available
• How eISF + Remote Site Access impacts every stage of the clinical operations lifecycle
• How to evaluate and select eISF + Remote Site Access platforms
• An inside look at the leading eISF + Remote Site Access platform in clinical trials