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
VIDEOS
Dive into the benefits of a site-first approach to technology and learn how empowering every site with integrated workflows can revolutionize your clinical trial process.
Florence eTMF is designed to give you all the capabilities you need in an intuitive and flexible interface. Plus, you get remote digital connection to 10,000 research sites managing their eISF on our network, with the ability to deploy the #1 digital site workspace to all of your study sites.
Florence SiteLink gives sponsors and CROs direct digital access to the network of 10,000 Investigator sites across 44 countries managing their eISF on our platform.
Florence eBinders integrates all of your clinical trial systems, automates eRegulatory processes, reduces contract negotiation time, tracks study progress, and enables secure remote monitoring on the industry-standard eRegulatory, eISF, and eSource 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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![GettyImages-1366661187 cell tech]( "How Technology Can Empower CAR T-Cell Therapy Clinical Trials")
Explore how innovative technologies are pushing advancements in CAR T-cell therapy, enhancing patient outcomes, and streamlining trial processes.
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![GettyImages-1182541081 data guidelines]( "Key Changes For Computerized Systems And Electronic Data")
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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![GettyImages-172361066 barriers]( "Breaking Down Barriers: Why Closed Technology Ecosystems Are Holding Back Clinical Research")
Explore the barriers created by closed technology ecosystems and the importance of open, interoperable solutions for advancing healthcare.
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![GettyImages-1132222912 dashboard]( "6 Ways Sponsors & CROs Are Optimizing Site Performance")
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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![GettyImages-1368094001 technology]( "Reducing The Chaos Of Technology Vendor Overload In Clinical Research")
Senior Innovations Business Analyst at Florence Healthcare, Beau Bruneau, shares three key insights from the Q1 2023 Florence Innovation Summit.
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![GettyImages-675233504 eregulatory]( "5 Steps To Overcome Barriers To eRegulatory Adoption")
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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![gettyimages-499785795 data linkage]( "Clinical Trial Technology Report Showcases 2023 Trends: Site Enablement, eISFs, And Integrations")
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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![Data Connectivity]( "How To Engage Frontier Sites Without Sacrificing Compliance Or Data Integrity")
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-european-union-flag-map]( "EU Annex 11: How To Stay Compliant")
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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![iStock-1245951271-compliance-regulation-quality]( "How Global Regulations Impact Technology: Shared Responsibility For Maintaining Compliance")
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.
