Clinical trials are crucial to the development and approval of new medications. Ensuring data integrity and patient safety throughout the process is a top priority. To address this, the European...
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The European Medicines Agency (EMA) periodically revises its guidelines to ensure that they remain relevant and up-to-date with the latest advancements in technology and industry best practices....
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By Catherine Gregor, Chief Clinical Trial Officer, Florence Healthcare As a dedicated clinical trial nerd, I have been closely following discussions around the FDA Omnibus Reform Act (FDORA)...
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The clinical research industry is evolving, especially when it comes to the adoption of technology. One of the first steps in making an impactful technology decision at your organisation is...
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The breakneck pace of new technology vendors entering the clinical trials space was the key focus during Florence's Q1 Innovation Summit, hosted by Florence’s Innovations Team of Andrea Bastek,...
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This is the first in a series of posts from Florence's Chief Clinical Trial Officer Andres Garcia on building better software for clinical trial operations. The clinical research industry is...
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Clinical trial management can be a daunting task, especially when you need to ensure that all your study sites are performing as they should. With so many moving parts, it can be challenging to...
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Saving time is crucial in clinical research. Falling behind schedule can delay regulatory approvals, miss patient recruitment opportunities, and even result in intellectual property loss. That's...
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Last week, the annual SCOPE Summit brought together leaders in the clinical research industry to discuss the latest trends and challenges. The conference highlighted the shifting power dynamic in...
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More than 250 companies create site, sponsor, and mobile technologies for clinical trials. Choosing between that many platforms can be overwhelming, especially when the average clinical research...
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Site Enablement refers to any technology that prioritizes the needs of clinical research sites. Site Enablement Platforms connect sites, sponsors, and CROs to enable continuous collaboration...
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Florence Healthcare just released the 2023 State of Clinical Trial Technology Report, with dozens of insights from more than 450 clinical research sites, sponsors, and CROs. We asked these...
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EU Annex 11 lays out the European Union’s regulations for using computerised systems during clinical trials. Any sponsor or site who wants their new medical treatment approved in the EU must...
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Since 2020, clinical research teams have radically changed how they approach clinical trial monitoring–and researchers need to adapt to this change to avoid being left behind. Before the...
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Decentralized clinical trials (DCTs) exploded in popularity after the COVID-19 pandemic, and they have now become a permanent part of the clinical trial landscape.
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Research sites and sponsors can’t stop talking about decentralized clinical trials (DCTs). But we often forget to ask a vital question: how do patients feel about them? As of 2021, 95% of...
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Patient retention in clinical trials is one of the largest challenges facing sites, sponsors, and CROs. The Center for Information and Study on Clinical Research Participation found that 23% of...
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When deciding on Clinical Research Coordinator (CRC) interview questions, research sites need to think about how the role is changing. Gone are the days when a Clinical Research Coordinator (CRC)...
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There are dozens of abbreviations for clinical trial terms. What’s the difference between a CRA, a CRC, and a CRO? How about the difference between eISF, ePRO, and eTMF? If you’ve been in medical...
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