
ABOUT FLORENCE HEALTHCARE
Florence Healthcare’s clinical trial software helps more than 12,000 research sites in 45 countries manage their documents, data, and workflows. The Florence Healthcare Site Enablement Platform™ also provides remote access so sponsors and Contract Research Organizations (CROs) can collaborate with their sites around the world. Florence Healthcare users now perform 5.8 million remote monitoring activities each month.
Florence’s Site Enablement Platform brings sponsor-site collaboration to life. By designing a platform around sites’ needs and enabling them to do their best work, Florence frees clinical trials from bottlenecks, so they can accelerate and scale.
BROCHURES
- Florence’s SiteLink™ Software For Sponsors And CROs
- Study Start-Up Shouldn’t Slow Your Trials Down
- Remotely Connect To Your Study Site’s eISF & Transform Your Clinical Trial Operations
- Streamline Clinical Operations With eTMF For Emerging BioTechs & Med Device Companies
- eRegulatory (eISF) Software For Clinical Research Sites
- Transform Your Operations With Florence's eTMF
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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Explore how innovative technologies are pushing advancements in CAR T-cell therapy, enhancing patient outcomes, and streamlining trial processes.
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Explore several modifications introduced in the updated guidelines by the European Medicines Agency (EMA) regarding computerized systems and electronic data in clinical trials.
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Explore the barriers created by closed technology ecosystems and the importance of open, interoperable solutions for advancing healthcare.
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See how Florence’s Site Enablement Platform works to overcome common trial hurdles and improve clinical trial operations, accelerate studies, and streamline compliance.
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Senior Innovations Business Analyst at Florence Healthcare, Beau Bruneau, shares three key insights from the Q1 2023 Florence Innovation Summit.
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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.