Read this guide for an in-depth overview of how eRegulatory and eSource are impacting clinical trials, and the steps teams can take to prepare now.
Explore how innovative technologies are pushing advancements in CAR T-cell therapy, enhancing patient outcomes, and streamlining trial processes.
Explore several modifications introduced in the updated guidelines by the European Medicines Agency regarding computerized systems and electronic data in clinical trials.
Explore the barriers created by closed technology ecosystems and the importance of open, interoperable solutions for advancing healthcare.
See how Florence’s Site Enablement Platform works to overcome common trial hurdles and improve clinical trial operations, accelerate studies, and streamline compliance.
Senior Innovations Business Analyst at Florence Healthcare, Beau Bruneau, shares insights from the Q1 2023 Florence Innovation Summit on how to choose the right technology.
Gain insight from this collection of best practices when transitioning from traditional paper and fragmented technology workflows to a fully electronic and purpose-built eRegulatory platform.
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.
By partnering with frontier sites, discover how sponsors and coordinating centers can make their trials more accessible and patient-centric.
EU Annex 11 lays out the European Union’s regulations for using computerized systems during clinical trials. Explore how sponsors and sites, who want their new medical treatment approved in the EU, must follow Annex 11.
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