How Sponsors & CROs can start-up and collaborate with “frontier” sites
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Multicenter Research
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Technology Can Help Sites and Sponsors Prepare for the Rapid Growth of Clinical Trials
The number of new clinical trials is expected to increase 5.8% each year from 2022 to 2030. But research sites already struggle to keep up with trial workloads. With 1,015 new trials starting in...
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Too Many Trials, Too Few CRAs: Closing the Capacity Gap in Clinical Trials
The clinical trial industry has experienced 5.8% annual growth year over year–but the growth in Clinical Research Associates (CRAs) and research sites isn’t keeping up. To accommodate the number...
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Too Many Trials, Too Few CRAs - Maximizing CRA Efficiency
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FDA Guidance for Diversity in Clinical Trials: What You Need to Know
The FDA’s newest guidance, “Diversity Plans to Improve Enrollment of Participants from Underrepresented Racial and Ethnic Populations in Clinical Trials,” took the clinical research world by...
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How Multinational Clinical Trials in the EU Can Benefit from Technology
Multinational clinical trials play an essential role in the European Union. In 2019 alone, Europe hosted 2,900 multinational trials. This was the second-highest number of clinical trials for any...
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5 Tips for Successful Decentralized Clinical Trials
Decentralized clinical trials (DCTs) –trials that don’t take place exclusively at major sites–have quickly grown in popularity. 89% of sponsors use DCT methods in some of their studies, and so do...
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Why Sites Must Own the eISF
Tell me if this sounds familiar: a sponsor needs remote access to their sites, so they buy electronic Investigator Site Files (eISFs) and distribute them to their sites. Now the sponsor has...
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How the New EU Clinical Trials Regulation Will Impact Sites and Sponsors
The Clinical Trials Regulation (CTR) for the EU took effect on 31 January 2022. Sites and sponsors must now embrace the new regulations to successfully run clinical trials across the European...
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What do the proposed changes to UK clinical trial regulations mean for you?
by Taylor Davidson, Content Writer With special thanks to Sara Guyler, Global Regulatory Specialist After leaving the European Union, the United Kingdom passed the Medicines and Medical Devices...
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Innovating Inclusive Study Startup and Recruitment | Florence Innovation Summit
This is a recording of our keynote panel during our Innovations Summit in Feb2022 discussing how the clinical research industry is innovating to focus on diversity and inclusion.
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9 Facts to Know About ICH E8(R1)
In October 2021, an event took place that the world had waited 25 years for: ICH E8 released its first revision. (Okay, maybe the world hadn’t been waiting—but the clinical research world had...
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Mount Sinai Success Story | Florence
Discover why Mount Sinai Health System chose Florence eBinders to streamline multi-center trial oversight.
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Overcoming Four Common Challenges in Multicenter Research
Overcoming 4 Challenges in Multicenter Clinical Trials Efficiently managing multicenter clinical trials is an essential capability of the modern research center. Complex protocols often require...
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Best Practices for Managing Multicenter Research
Learn how to streamline your multicenter research with best practices from your peers.
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Technology in Multicenter Clinical Trials
Managing and Organizing Multicenter Clinical Trials with Technology Are you part of a multicenter clinical trial? If not, you may be soon. Multicenter clinical trials, where a sponsor or CRO...
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