The role of a Clinical Research Associate (CRA) changed dramatically during the pandemic. 76% of CRAs did most of their monitoring visits remotely in 2020, up from just 18% in 2019. And technology...
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Clinical Research Coordinators (CRCs) play a crucial role in the success of research sites. With a wide range of responsibilities, the CRC is the “heart” of a clinical trial—the champion of the...
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The New Standard for CROs 80% of sponsors and Contract Research Organizations (CROs) expect study start-up, recruitment, consenting, source data collection, and monitoring to be mostly digital by...
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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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By Blake Adams, VP of Marketing and Growth for Florence 90% of clinical trial sponsors rely on some form of remote monitoring. This statistic makes reliable, efficient remote site access more...
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75% of research sites either already use eConsent or plan to use it in the near future. That means the question is no longer “does my site need eConsent?” but “which eConsent platform do I need?” ...
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The Next Phase Podcast: Exploring Innovation in Clinical Trials
SubscribeBy Blake Adams, VP of Marketing at Florence 75% of research sites either already use electronic informed consent or plan to use it in the future. Sites without this technology will quickly fall...
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By Charlotte Boyd, Sr. Manager, Community and Customer Marketing, Florence The explosion in remote clinical trial technology over the past two years has changed how clinical research teams work...
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How Cybersecurity Protects Participants in Clinical Trials Special thanks to Zack Wilkinson, Information Security Manager at Florence, for his contributions to this article. Cybersecurity in...
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Contract research organizations (CROs) play a vital role in clinical trials. The CRO market was worth $61 billion in 2020 and is expected to reach $99 billion in 2026. In the midst of the...
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by Kathryn Meagley, Senior Product Manager at Florence and former Clinical Research Manager at the Atlanta Veterans Affairs Medical Center Historically, informed consent in clinical trials has...
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Over the past 10 years, the number of oncology clinical trials has grown almost twice as fast as the number of trials for any other disease. Oncology trials are a vital source of income for...
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by Andrea Bastek, PhD, Director of Innovation at Florence and Former Senior Field Clinical Engineer at Abbott 75% of research sites either have some form of eConsent or want to adopt an eConsent...
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Clinical trial site management costs sponsors and CROs millions of dollars each year. One report estimated that completed clinical trials cost between $44 million and $115 million each. Of those...
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eConsent, software that lets trial participants read and sign informed consent documents online, has exploded in popularity. As of July 2021, 57% of research sites use eConsent applications, and...
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Clinical trial sites embraced remote patient engagement technology in 2020 and 2021. 95% of research sites now offer telemedicine visits, while 94% use electronic patient diaries and 91% use...
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This is a modified version of an article that first appeared in STAT. Check out the original here. In the midst of battling a pandemic, healthcare professionals are also battling burnout and...
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Successful, sustainable companies must balance growing quickly with supporting and valuing their employees. That’s why Florence was thrilled to receive several awards for building a great place to...
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Research sites struggle with patient diversity in their clinical trials, and this can have a negative impact on treatment outcomes. In 2018, African American people made up 13.4% of the U.S....
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Many clinical trial sites want to use technology but worry about compliance, especially 21 CFR Part 11 compliance. Using technology that isn’t compliant can lead to audits and stressful...
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