
ABOUT FLORENCE HEALTHCARE
Florence Healthcare’s clinical trial software helps more than 18,000 research sites in 52 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
- Transform Your Clinical Trial Operations
- Electronic Informed Consent For Clinical Research
- A Definitive Guide To The Site Enablement Maturity Assessment
- eISF: Industry Standard eRegulatory Software For Clinical Sites
- Site Enablement Platform For Top Biopharma
- Study Start-Up Shouldn't Slow Your Trials Down
- eTMF Software For Fast-Growing Biotech
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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Critically examine prevalent myths surrounding electronic Trial Master Files (eTMFs) and their integration with electronic Investigator Site Files (eISFs).
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In 2025, it is likely the clinical trial landscape will be shaped by advancements in artificial intelligence (AI), evolving recruitment strategies, and a renewed focus on equitable access.
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A study of how leading research centers, CROs, and sponsors cover the cost of eRegulatory tools... and then some.
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A well-maintained TMF, supported by digital solutions, is the backbone of successful clinical trials, improving trial management and readiness for audits or regulatory submissions.
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Explore the FDA's 2024 final guidance on DCTs, including key updates that address previous concerns, affecting healthcare providers, sub-investigators, and sponsors.
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See how study management tools simplify clinical trial management by centralizing all study information, enhancing efficiency and precision, and more.
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By addressing the unique hurdles tied to regulations in European clinical trials, eBinders offer a streamlined approach to managing electronic trial documentation.
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Consider several forward-looking strategies shared by industry leaders that can also serve as a valuable resource for professionals navigating the complex terrain of clinical research collaboration.
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Learn why collaboration and interoperability are crucial to breaking down barriers, embracing innovation, and creating a future where clinical research operations are more efficient, effective, and patient-centric.
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Delve into the pivotal role played by this Site Enablement Platform in upholding business continuity for clinical trials.