5 Essential Steps To Remote Site Access

by D'Anna Siegle, Senior Product Marketing Manager, Florence

Sites, sponsors, and CROs now perform the bulk of their clinical trial operations by logging into cloud-based systems. The 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.

As a sponsor or CRO, taking advantage of these new opportunities for eISF integrated remote site access is essential to streamline your clinical operations.

An eISF integrated remote site access solution connects disjointed site platforms, such as the CTMS, EMR, EHR, eRegulatory, eSource, and eConsent, to a single point of access for the sponsor/CRO.

This approach to remote collaboration drives high engagement rates at study sites because the solution is purpose-built to streamline their internal workflows and be usable across all of their studies.

Our extensive experience working with over 7,200 study sites and facilitating remote monitoring for more than 400 sponsors and CROs gives us insights across the industry for what makes an integrated remote site access strategy work.

As you evolve your monitoring and site management strategy to a remote approach, we are providing you with the 5 essential considerations to focus on to ensure site acceptance, site adoption and a successful implementation of your remote strategy.