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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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.
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Unearth how embracing these specific approaches ensures that technology becomes a true ally in enhancing precision, accessibility, and collaboration within the intricate realm of clinical research.
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Learn how sites can enhance their ability to meet start-up timelines, positively impacting both operational efficiency and patient outcomes.
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Read this guide for an in-depth overview of how eRegulatory and eSource are impacting clinical trials, and the steps teams can take to prepare now.
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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 regarding computerized systems and electronic data in clinical trials.