eSource and eCTD Guidance & Eliminating Shadow Charts: Is Now the Time?
Shadow charts develop for various reasons in clinical research as discussed in a prior post on shadow charts. They emerge at trial sites because of disparate IT systems: for example an EHR record may...
View ArticleLeading Prostate Cancer Research Organization Partners with Florence
PCCTC Collaborates with Florence Healthcare to Enhance Regulatory Document Management Capabilities ATLANTA, GA and NEW YORK, June 10, 2016 – Florence Healthcare, developer of the innovative trial...
View ArticleDefining eSource for Clinical Trials: Three Practical Categories
When discussing eSource there is as much detail to explore as any other segment of clinical trial operations. But from small biotechs to top 20 pharma, the starting point for discussions is more...
View ArticleFlorence Featured in FierceBiotech
Florence Healthcare snags cash to switch trial sites from paper to the cloud Florence Healthcare has picked up seed funding to help clinical trial sites switch from paper files to the cloud. The...
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What does a modern Clinical Research Coordinator do?
What does a modern Clinical Research Coordinator do?Clinical research coordinators (CRCs) play a crucial role in ensuring the success of research sites. Managing a myriad of responsibilities throughout...
View ArticleMy clinical trial monitors say they don’t want an electronic binder. What do...
The transition to electronic clinical trial binders (eBinders or investigator site files) is underway across the clinical research industry. eBinders provide several advantages for your site....
View ArticleFlorence Healthcare Wins DPharm Idol 2016
Emerging technology company chosen as the most innovative in clinical research at Disruptive Innovations 2016. Atlanta, Ga- Florence Healthcare, a software platform company focused on improving...
View Article4 Takeaways from the 4th Annual Embracing Change Conference for Clinical...
The 4th Annual Embracing Change Conference for Clinical Research was a well-produced event from Arizona State University’s Clinical Research Management program. If you did not make it and would like a...
View Article“My PIs are super busy and unable to try new things! How can I convince them...
Research protocol complexity is increasing and trial volumes are growing. The result – sites are struggling to take on more with the same team. Physicians and research teams are overwhelmed with...
View ArticleWhat if I get audited?
A common question many teams ask as they face the transition to digital study documents is, “What if I get audited?” Inspections evoke fear because negative audit findings significantly impact...
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What’s Your eRegulatory Strategy?
What’s your eRegulatory Strategy? In the last year we’ve met with dozens of research teams to discuss this question. In the process, we’ve discovered that moving to an eRegulatory platform is much more...
View ArticleFlorence Nominated to Present at 2017 Montgomery Summit
Florence, the company advancing clinical research through software, will be presenting at the 2017 Montgomery Summit this week in Santa Monica California. The Montgomery Summit chose Florence to...
View ArticleCan 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...
View ArticleeClinical 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...
View Article5 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...
View ArticleYour 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...
View ArticleYour 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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