Featured Articles
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Key Changes For Computerized Systems And Electronic Data
5/24/2023
Explore several modifications introduced in the updated guidelines by the European Medicines Agency regarding computerized systems and electronic data in clinical trials.
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Breaking Down Barriers: Why Closed Technology Ecosystems Are Holding Back Clinical Research
5/24/2023
Explore the barriers created by closed technology ecosystems and the importance of open, interoperable solutions for advancing healthcare.
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6 Ways Sponsors & CROs Are Optimizing Site Performance
5/11/2023
See how Florence’s Site Enablement Platform works to overcome common trial hurdles and improve clinical trial operations, accelerate studies, and streamline compliance.
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Clinical Trial Technology Report Showcases 2023 Trends: Site Enablement, eISFs, And Integrations
1/17/2023
Dive into six insights to stay on top of the rapidly shifting research industry and to ensure your research organization doesn’t get left behind.
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EU Annex 11: How To Stay Compliant
11/16/2022
EU Annex 11 lays out the European Union’s regulations for using computerized systems during clinical trials. Learn how sponsors and sites seeking treatment approval in the EU must follow Annex 11.
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How eConsent Can Help Legally Authorized Representatives
6/22/2022
Software vendors often forget to think about the needs of LARs, even though they play a vital role in clinical trials. Explore three ways eConsent can help LARs complete the informed consent process.
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7 Key Findings From A Clinical Trial Operations Technology Survey
1/19/2022
To stay competitive in the clinical research field, sites, sponsors, and CROs need to invest in remote technology. Discover seven key trends that your clinical trial team needs to know about.
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Study Start-Up Checklist For Digital Clinical Trials
Read how five Florence employees with clinical research backgrounds came together to craft a checklist designed to walk sites through the process of tech-enabled study start-up.