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Transitioning Your CRA Team to Digital Site Management
Over the last six months something interesting happened in usage data for eBinders, Florence’s eRegualtory and eSource platform, and by extension for study management in general. In April 2018 Clinical...
View ArticleNontransferable Obligations: Why Sponsors Fail Inspections
Part 1: Lack of Oversight Discussion of FDA inspections, whether for cause or part of a routine GCP inspection, usually centers on the inspection of trial sites and the CROs who are tasked with...
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Ten Must-Have Capabilities When Evaluating eRegulatory Platforms
Successfully transitioning your team to an eRegulatory solution, while avoiding costly compliance mistakes and realizing true time-saving benefits, requires careful evaluation of potential platforms....
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Florence Named to Top 100 Places to Work in Atlanta
Atlanta, GA, September 10, 2018 (Newswire) – Florence, a fast-growing Atlanta based company building software that advances clinical research, has been named one of the top 100 Best Places to Work in...
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Ten Ways Florence eBinders™ Accelerates Study Startup
Moving to an eRegulatory/eSource solution generates measurable impact on clinical trial study startup timelines. Research teams reduce startup time by as much as 40% through harnessing the built-in...
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Four Observations from Site Solutions Summit
This year’s SCRS Site Solutions Summit was the biggest ever, and for good reason—sites are coming into their own in the clinical trial value chain. Not only are sites maturing their operations and...
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Key Expectations of Clinical Trial Operations Leaders in 2019
Today’s clinical trial operations leaders are in a challenging and expanding role. You are expected to increase study capacity, manage more complex trial protocols, accelerate study startup, and ensure...
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Thank you for a great 2018!
What a great year at Florence! As we look back and celebrate all that has happened this year on our mission to advance research, we thank you for being a part of the Florence family. We are excited to...
View ArticleHow Lauren Begnaud Transitioned 65 Sites to eRegulatory at US Oncology
In this interview, we talked with Lauren Begnaud, Manager of Regulatory Affairs at the US Oncology Network, to discover how she successfully migrated 65 trial sites, 400 studies, and 2,000...
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Observations from TMF Summit 2019: The Post-eTMF World
The Florence team just returned from the 2019 TMF Summit in Orlando, and interestingly, the core conversations throughout the conference were not really about TMFs. The innovation frontier in our...
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5 Key Advantages of eRegulatory
Over 75% of clinical trial sites who have not yet adopted eRegulatory plan to do so in 2019. Why? In addition to growing industry pressure from sponsors who expect a digital site infrastructure, trial...
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ALCOA-C in Clinical Trial Electronic Document Management
Good documentation is vital to good clinical research. As the saying goes, “If it isn’t documented, it doesn’t exist”. In fact, one of the most common inspection findings in investigator site...
View ArticleFDA: Technology’s Value in a World of Precision Medicine and Research
Over the course of the past 10 years, significant advancements have been made in clinical research. Personalized medicine, immunotherapies and genomic testing have equipped researchers with the tools...
View ArticleTechnology in Multicenter Clinical Trials
Managing and Organizing Multicenter Clinical Trials with TechnologyAre you part of a multicenter clinical trial? If not, you may be soon. Multicenter clinical trials, where a sponsor or CRO relies on a...
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Integrating the eTMF and eISF: Why and Why Now?
Best Practices for eISF and eTMF IntegrationElectronic Investigator Site Files (eISF) are now attracting the attention of progressive sponsors and CROs. Here, we’ll explore the different approaches and...
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Overcoming Four Common Challenges in Multicenter Research
Overcoming 4 Challenges in Multicenter Clinical TrialsEfficiently managing multicenter clinical trials is an essential capability of the modern research center. Complex protocols often require diverse...
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Why Remote Clinical Trial Monitoring is the New Standard
Why Remote Clinical Trial Monitoring is the New StandardThe COVID-19 pandemic has accelerated the ongoing shift to remote clinical trial monitoring. Remote site access and monitoring platforms are now...
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