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Florence Healthcare Joins Clinical Trials Transformation Initiative
Atlanta, Georgia, July 6, 2022–Florence Healthcare, a clinical trial software company that serves as the digital link between research sites, sponsors, and CROs, has joined the Clinical Trials...
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Technology Can Help Sites and Sponsors Prepare for the Rapid Growth of Clinical Trials
The number of new clinical trials is expected to increase 5.8% each year from 2022 to 2030. But research sites already struggle to keep up with trial workloads. With 1,015 new trials starting in...
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Tips for a successful clinical research software implementation
It’s clear that remote work is here to stay. For industries like healthcare that have historically relied on in-person interactions and paper-based records, this means implementing new digital...
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Battling Turnover with Clinical Trial Career Development
By Andrea Bastek, PhD, Senior Director of Innovation at Florence Whether you’re a Clinical Research Associate, Research Assistant, or Clinical Research Coordinator, working in the clinical trial...
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How to Reduce Operational Costs of Clinical Trials in Uncertain Economic Conditions
Clinical trials can’t avoid fluctuating economic conditions. Changes in the market can especially impact emerging and early-stage biotech companies with limited cash reserves. A clinical trial's...
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Too Many Trials, Too Few CRAs: Closing the Capacity Gap in Clinical Trials
The clinical trial industry has experienced 5.8% annual growth year over year–but the growth in Clinical Research Associates (CRAs) and research sites isn’t keeping up. To accommodate the number...
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Too Many Trials, Too Few CRAs - Maximizing CRA Efficiency
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FDA Guidance for Diversity in Clinical Trials: What You Need to Know
The FDA’s newest guidance, “Diversity Plans to Improve Enrollment of Participants from Underrepresented Racial and Ethnic Populations in Clinical Trials,” took the clinical research world by...
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Remotely Manage Document Workflows with SiteLink
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Breaking Down the FDA's 2022 Guidance on Diversity
Learn from Catherine Gregor about the newly published FDA draft guidance for increasing participant enrollment from underrepresented racial and ethnic groups in clinical trials.
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How Multinational Clinical Trials in the EU Can Benefit from Technology
Multinational clinical trials play an essential role in the European Union. In 2019 alone, Europe hosted 2,900 multinational trials. This was the second-highest number of clinical trials for any...
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5 Tips for Successful Decentralized Clinical Trials
Decentralized clinical trials (DCTs) –trials that don’t take place exclusively at major sites–have quickly grown in popularity. 89% of sponsors use DCT methods in some of their studies, and so do...
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The Impact of Remote Site Monitoring on Clinical Research Associates | Florence Benchmark Report 2022
A benchmark report of 143 global Clinical Research Associates (CRAs) who conduct remote monitoring through a digital link to the research site’s electronic Investigator Site File (eISF).
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4 Trends in Clinical Research You Need to Know About from ACRP 2022
Wondering what’s next in the world of clinical research? Catherine Gregor, Florence’s Chief Clinical Trial Officer and the former Director of Clinical Research Administration at Vanderbilt,...
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Why Sites Must Own the eISF
Tell me if this sounds familiar: a sponsor needs remote access to their sites, so they buy electronic Investigator Site Files (eISFs) and distribute them to their sites. Now the sponsor has...
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How Digital Connections Can Create a Positive Patient Experience in Clinical Trials
Patient experience in clinical trials is a problem. On patient satisfaction surveys, clinical trials received low scores similar to the scores of Internet service providers, utility companies, and...
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How the New EU Clinical Trials Regulation Will Impact Sites and Sponsors
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...
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Why Sponsors and CROs Are Investing in Electronic Investigator Site Files for Their Sites in 2022
The first three months of 2022 have seen a 3x uptick over the first three months of 2021 in clinical trial sponsors and CROs contacting Florence about deploying Electronic Investigator Site Files...
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How Community-Based Clinical Trials Benefit Sponsors, Local Healthcare Systems, and Patients
Clinical trials could help far more patients than they currently do. So how do we expand studies to all of the patients who need them? Community-based clinical trials might be the answer. 70% of...
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