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Can I control access with electronic binders?
You’ve decided to make the transition from papers to digital. Your sponsor is on board. You’ve organized your binder and folder structure templates. Now what? It’s time to configure access by setting...
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eClinical tools to dClinical tools
Gartner’s Michael Shanler was one of the first to recognize the trend of dClinical. He noticed that a new generation of software vendors was emerging who handled project management and reporting in a...
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5 Ways To Engage Clinical Trial Sites With Technology
As Featured in Clinical Leader, July 13 2017 Clinical research has a reputation for being notoriously slow to adopt new technologies. This should come as no surprise to those in the industry, since we...
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Your Roadmap to eRegulatory: Establishing Goals
Transitioning to an eRegulatory platform is full of benefits; accelerated study startup, centralized document management, the ability to review and sign documents anywhere, easy task management, remote...
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Your Roadmap to eRegulatory: Define Eight Critical Workflows
Transitioning to an eRegulatory platform is full of benefits; accelerated study startup, centralized document management, the ability to review and sign documents anywhere, easy task management, remote...
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“I have too many systems!”| The Top 4 Integrations You Need
New technology should accelerate your studies, however, for many research sites new technologies end up adding complex and redundant processes for your team. Avoiding these additional processes...
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Innovations | The time is now for eRegulatory and eSource
Innovation matters in Clinical Research…The adoption of new technology, in any industry, follows a familiar cycle outlined by Geoffrey Moore in his book Crossing the Chasm, Innovators: Innovators are...
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Florence Named to TAG Top 40
ATLANTA, GA – February 21, 2018 – Florence was named one of the Top 40 Innovative Technology Companies in Georgia by the Technology Association of Georgia (TAG). TAG’S Top 40 Awards recognize...
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Cancer Research Is Accelerating, But We Can Do Better
The rate of cancer death has been decreasing, and people are living longer with cancer than ever before. Approximately 64% of US patients diagnosed with cancer in 2005 have lived 10 years or more...
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How to Use Electronic Signatures (eSignatures) in Clinical Trials
Electronic signatures, eSignatures, are continuing to gain momentum replacing wet signatures in Clinical Trials. Wet signatures are signatures made by hand on a document, typically with a pen and...
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The Impact of Remote Monitoring on CRAs | Central Monitoring Summit
While presenting at Central Monitoring Summit 2018, Elizabeth Robinson of Horizon Pharma shared a strong data point: In the coming years, Clinical Research Associates (CRAs) will experience more change...
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5 Things to Know about Blockchain and Clinical Trials
“Blockchain will change the world!” This is the common message found in search engines and blog posts across the internet. But really, how many times have you heard this message before? It seems that a...
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Webinar | Solving Clinical Trial Inefficiencies with eRegulatory
Webinar: Solving Clinical Trial Inefficiencies with eRegulatoryIn this on-demand webinar our team examines how leading clinical trial sites are solving clinical trial operation inefficiencies with...
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Webinar | Blockchain and Clinical Trials
Webinar: Blockchain and Clinical TrialsWatch this on-demand webinar as our Chief Technology Officer explores the impact of Blockchain on Clinical Trials, and if you should be planning for it at your...
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10 Superpowers of Clinical Trial Leaders
While helping over 10,000 research teams migrate Florence eBinders for eRegulatory, we’ve encountered people who have become “superheroes” in managing the workflow of regulatory and source documents at...
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Webinar | Surviving an FDA Inspection with eRegulatory
On-Demand Webinar: Surviving an FDA Inspection with eRegulatoryIn this recorded webinar our panel of experts from Florence and LMK Clinical Research discuss how an FDA inspection works with...
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How to Avoid the Top 5 Clinical Trial FDA Inspection Failures
Your heart begins beating faster and sweat begins forming on your forehead – the FDA is calling. Many things can trigger an FDA inspection – most falling into routine study-related visits, while some...
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Webinar | Avoiding Digital Site Surprises
Recorded Webinar: Avoiding Digital Site SurprisesOdds are that your CRA team is already logging into electronic investigator site files at some of your sites. Now what? View this on-demand webinar to...
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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...
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Nontransferable 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...
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How 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...
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FDA: 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...
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Technology 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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4 Ways Site Enablement Platforms Support The White House’s Call for a...
4 Ways Site Enablement Platforms Support The White House’s Call for a Stronger Clinical Trial InfrastructureThe White House Office of Science and Technology Policy (OSTP) recently announced the launch...
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Florence @ SCOPE 2024
Florence @ SCOPELooking to boost site adoption of your clinical innovations? Insights await at the Florence booth. Our experience with 18k sites across 50+ countries and partnerships with over 3,200...
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