Featured Articles

  1. Why Remote Site Monitoring Is On The Rise And How To Deploy It At Your Organization 1/12/2021

    The COVID-19 pandemic has accelerated the ongoing shift to remote clinical trial monitoring. In this article, we explore challenges of traditional monitoring, benefits of remote clinical trial monitoring, how to deploy remote clinical trial monitoring, sponsor-deployed remote monitoring technology, and site-procured remote monitoring technology.

  2. 2021 State Of Clinical Trial Technology Industry Report 1/4/2021

    How are clinical operations leaders making strategic technology investments in 2021 and beyond? This report provides insights from more than 200 respondents to the annual Florence State of the Industry Survey, from dozens of stakeholders who are members of the Florence Executive Advisory Board, and more than 8,500 study sites and more than 8,000 sponsors using Florence.

  3. How Remote Site Access Eliminates Clinical Trial Bottlenecks 12/14/2020

    Sites, sponsors, and CROs now perform the bulk of their clinical trial operations by logging into cloud-based systems. Direct digital connectivity and collaboration access with your sites, via connecting to the largest Electronic Investigator Site Files (eISF) in research, eliminates clinical trial bottlenecks.

  4. 7 Misconceptions About Managing Your Clinical Research In The Cloud 12/14/2020

    In a world with more data and less time, the advantages of cloud-based technologies are hard to ignore. Debunk some of the common misconceptions of managing clinical research documents, data and workflows in a cloud-based technology platform.

  5. Why Open APIs Are Critical For Clinical Trial Software 12/14/2020

    Today’s modern clinical trial requires robust and purpose-built eClinical solutions. One of the essential capabilities you must ensure exists is the ability to integrate with other systems through Open APIs.

  6. How To Create A Digitally Connected Clinical Trial Ecosystem 11/18/2020

    Sponsors and CROs’ ability to access and collaborate with a research site is essential to the success of every study. As study sites “come on-line,” Sponsors and CROs are in a unique position to harness this digitally connected network of sites to turn on remote site access and Source document review/verification (SDR/V), and streamline workflows. In this article, we examine the key quality outcomes and technology recommendations associated with digitally accessing the site eISF.

  7. Six Reasons Why Sites Should Use The eISF Reference Model 11/18/2020

    The Electronic Investigator Site File (eISF) Reference Model is the industry standard for setting up and managing an Electronic Investigator Site File. 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. Here are six benefits of an eISF Reference Model.

  8. 5 Essential Steps To Remote Site Access 9/28/2020

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

  9. Seven Things Your Remote Monitoring Solution Needs To Ensure Success With Study Sites 9/16/2020

    Remote site monitoring platforms are now a requirement in clinical research operations. While accelerated to mitigate COVID disruptions to site-access, the pivot to remote site access will be the new normal. This article highlights how to select the remote site monitoring solution for your clinical trial.

  10. Your eTMF And Your Study Sites: How To Close The Document Gap 9/8/2020

    Not all sponsors and CROs that select and implement an Electronic Trial Master File (eTMF) solve the bottlenecks and inefficiencies that the system was selected to target. Why? Often, during the vendor selection process, organizations undervalue the need for site acceptance, disregard the impact of vendor support teams, overlook critical implementation processes, and don’t fully understand the correlation between software capabilities and the bottlenecks they address. This article addresses some common friction points and how to address them.