Your Guide to Preparing an Annual Clinical Trial Site Budget
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eConsent
Explore all Florence eConsent content.
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How to Prepare Your Annual Capital Expenditure Site Budget for Scalability
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What does a modern Clinical Research Coordinator do, and how can technology help?
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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How to De-Risk Your Move to eConsent Webinar
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Top Considerations When Choosing eConsent Software
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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Six Ways to De-risk eConsent for Sites
By 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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How Cybersecurity Protects Participants in Clinical Trials
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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How to Scale Clinical Trials with Technology
Industry veteran, Rebecca Kush, PhD, Chief Scientific Officer of Elligo Health Research, explores the big picture of implementing and operationalizing key clinical research technology.
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The Life Cycle of Informed Consent in Clinical Trials
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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The Challenges of Oncology Clinical Trials (and How Tech Can Help)
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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The Benefits of eConsent Forms for Clinical Trials
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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What is eConsent
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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Florence eConsent Capability Evaluation Checklist
Use this checklist to evaluate electronic consent solutions and determine what you need to ask vendors to reach your goals.
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How to use patient engagement technology in your clinical trials
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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Digital Research at Clinical Trial Sites: 2021 Mid-Year Survey Report
Learn about the latest trends in digital research technology from our 2021 mid-year report.
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How eConsent Powers More Participant Engagement in Clinical Trials
This article is written by Angela Gill Nelms and was originally published on medcitynews.com here. The chances are high that you have signed at least one consent document in your life. Consents...
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