Florence Mobile App for Sponsors
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Site Enablement refers to any technology that prioritizes the needs of clinical research sites. Site Enablement Platforms connect sites, sponsors, and CROs to enable continuous collaboration...
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Florence Healthcare just released the 2023 State of Clinical Trial Technology Report, with dozens of insights from more than 450 clinical research sites, sponsors, and CROs. We asked these...
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Learn How Florence eConsent will Simplify Your Consent Process
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Take The TourATLANTA - January 11, 2023 - Florence Healthcare™, a clinical research technology company, has released its annual State of Clinical Trial Technology Report. Over four hundred clinical research...
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Learn about the future of consenting, how focusing on patient engagement drives decisions for Sponsor of Choice, and the critical features you don't want to leave out of your eConsent tool.
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Patient retention in clinical trials is one of the largest challenges facing sites, sponsors, and CROs. The Center for Information and Study on Clinical Research Participation found that 23% of...
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Whether you’ve already gone digital, or are just starting to transition, join us as we dive into the future of consenting.
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Patient-facing technology can make trials more accessible and help trials fit into participants’ lives. But if we’re not careful, technology built to empower patients may end up overwhelming them...
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When clinical trial sites, sponsors and tech vendors think about diversity and inclusion, we consider a variety of factors: age, race, ethnicity, gender identity, sexual orientation, ability, and...
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The number of clinical trials has increased rapidly since 2020. 2021 saw a 14% increase in trial starts over 2020 and a 19% increase over 2019. And while 2020 was far from a typical year, the...
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A legally authorized representative (LAR) has a vital role to play in clinical trials, yet clinical trial software vendors too often forget to think about LARs and their needs. Most clinical...
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Access a personalized on-demand tour of the Florence eBinders platform
Take The TourThe 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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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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ATLANTA–(Business Wire)--The first research site to adopt Florence eConsent has successfully registered 250 patients after just 30 days of using the platform. Florence designed eConsent to speed...
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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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Florence eConsen: An Interview with Mason McLellan with CEDAR at OHSU Knight Cancer Institute sharing why their organization moved to eConsent, how they did it and the impact it’s making.
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Florence eConsent: An Interview with Morgan Oats at Levine Cancer Center sharing why their organization moved to eConsent, how they did it and the impact it’s making.
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