Six Reasons Why Sites Should Use The eISF Reference Model

The Electronic Investigator Site File (eISF) Reference Model is the industry standard for setting up and managing an Electronic Investigator Site File. The model was designed by leading research sites and sponsors, along with all of the major eISF vendors.

The 2020 Florence State of the Industry Report projects the Electronic Investigator Site File (eISF) to be in use at over 61% of clinical research Sites by the end of 2020. At the same time, clinical trials continue to become increasingly collaborative – especially with the rise of multi-center trials that require various research sites across different organizations to work together.

The rise in the eISF, coupled with an increasing need for real-time collaboration and document exchange among sites and sponsors/CROs, mandates the need for an eISF Reference Model.

Leading eISF vendors dedicated their resources to collaborating with other vendors in the space to develop universal guidance. Sites have the freedom to select the eISF platform that best fits their needs without fear that there will be diminished collaboration opportunities with external stakeholders.

Here are six benefits of an eISF Reference Model.