
ABOUT FLORENCE HEALTHCARE
Florence accelerates clinical research with innovative solutions to streamline clinical trial site workflows and remote connect sponsors, CROs, and sites for access, monitoring, management, and SDR/V. The Florence platform is the industry standard with more than 10,000 research sites in 45 countries, sponsors and CROs collaborating on its network.
Research study sites manage their internal document operations with the #1 Electronic Investigator Site File with solutions across eRegulatory, Source Capture, eConsent, eLogs, Contract Management, SOP Management, and Remote Access.
Sponsors and CROs gain unprecedented remote access to their study sites for remote startup, monitoring, and SDV built on the industry-standard remote site access platform.
CONTACT INFORMATION
Florence Healthcare
600 Peachtree St. NE, Suite 920
Atlanta, GA 30308
UNITED STATES
Phone: 706-768-2196
Contact: Blake Adams
FEATURED ARTICLES
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Gain insight from this collection of best practices when transitioning from traditional paper and fragmented technology workflows to a fully electronic and purpose-built eRegulatory platform.
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Dive into six insights to stay on top of the rapidly shifting research industry and to ensure your research organization doesn’t get left behind.
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By partnering with frontier sites, discover how sponsors and coordinating centers can make their trials more accessible and patient-centric.
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EU Annex 11 lays out the European Union’s regulations for using computerized systems during clinical trials. Explore how sponsors and sites, who want their new medical treatment approved in the EU, must follow Annex 11.
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When searching for clinical trial software, every site, sponsor and CRO has the same question: “how does this software comply with (insert clinical trial regulation here)?” Learn the answers in this article.
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This article breaks down what sites and sponsors need from site feasibility and how a unified site-sponsor platform can address these needs and improve collaboration.
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This article covers what the “patient experience” is in clinical trials, the problems with the patient experience in clinical trials, and four ways digital connections can create a positive patient experience in clinical trials.
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The clinical trial industry has experienced 5.8% annual growth year over year–but the growth in CRAs and research sites isn’t keeping up. How can we close these capacity gaps, when most sites already have more trials than they can handle and there are ongoing CRA shortages? We must innovate.
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Learn how a top 3 global CRO implemented technology to remotely connect with their research sites and can now monitor up to 50 sites per week, compared to the former average of two on-site monitoring visits per week.
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In this article, discover how remote site collaboration platforms can help sponsors weather economic fluctuations when it comes to clinical trials.
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Delve into how repairing the broken links between sites, sponsors, and CROs can save the 22% of trials that fail due to lack of funding, resulting in hundreds of new treatments to patients faster.
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In this article, explore the three ways eConsent can help a legally authorized representative (LARs).
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While diversity, equity, and inclusion have been major focuses for clinical research teams, sponsors and sites were excited to receive explicit FDA guidance in April 2022. But what do clinical research teams need to know from the guidance, and how can they prepare to incorporate it?
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As of April 2022, ICH E8(R1) is officially in effect. Since ICH E8(R1) revolves around study design, a deep understanding of the new guidelines to create study protocols is needed. Discover key takeaways for organizations that design protocols and run clinical trials.
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The Clinical Trials Regulation (CTR) for the EU took effect on 31 January 2022. Sites and sponsors must now embrace the new regulations to successfully run clinical trials across the European Union.
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Learn how the end result to decentralized trials is greater patient-centricity, higher enrollment, fewer drop-outs, and a faster study timeline.
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Once you’ve implemented a new software or process into your clinical trial organization, you may find yourself asking, “Now what?” The answer to that is simple: focus on change management.
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Read how five Florence employees with clinical research backgrounds came together to craft a checklist designed to walk sites through the process of tech-enabled study start-up.
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Discover 7 key trends in clinical operations technology that your clinical trial team needs to know about.
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In the available article, read about the three common concerns about going paperless with clinical research.