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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On-Demand Webinar: Finding the Missing Link to Decentralized Trials
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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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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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Access TourContract 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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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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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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Where should you start if you are managing a multi-center study, grant-funded study, or Investigator-Initiated Trial in an eTMF? Find out in this complimentary webinar.
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Learn how a global leader in neurodegenerative disease research streamlines document exchange with more than 50 research sites through Florence.
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Learn about the latest trends in digital research technology from our 2021 mid-year report.
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The study start-up process overflows with important but stressful tasks. Research sites need to determine whether a study is feasible and convince a sponsor to select them for the study. Then...
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Decentralized clinical trials have exploded in popularity. A WCG survey showed that 94% of research sites have adopted at least one decentralized method, and 88% of sites have already hosted...
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As decentralized clinical trials become more popular, many sites and sponsors have begun to wonder how they can adopt decentralized methods without sacrificing compliance or efficiency. The...
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Read our extensive checklist on everything you need to consider regarding FDA 21 CFR Part-11 compliance for clinical trial electronic document management and workflows.
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Decentralized trials isn't just a buzzword. Learn how this model will have a major impact on sites and clinical trial operations.
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Learn how sites and sponsors can plan their technology strategies today for the clinical trials of tomorrow.
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Find out how Florence partnered with the Center for International Blood and Marrow Transplant Research to migrate 10 ongoing studies and 100 sites from a legacy eTMF to Florence in 8 weeks.
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Wondering which eTMF software has all the features you need to run successful clinical trials? Use this checklist to evaluate eTMFs and choose the one that's right for your team.
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We've gathered everything you need to know about choosing and implementing an eTMF into a single eBook. Download it before you choose an eTMF, or to get the most out of the eTMF you already have.
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