Wondering what’s next in the world of clinical research? Catherine Gregor, Florence’s Chief Clinical Trial Officer and the former Director of Clinical Research Administration at Vanderbilt,...
Read Blog
Read Blog
ATLANTA–(Business Wire)--The first research site to adopt Florence eConsent has successfully registered 250 patients after just 30 days of using the platform. Florence designed eConsent to speed...
Read Blog
Patient experience in clinical trials is a problem. On patient satisfaction surveys, clinical trials received low scores similar to the scores of Internet service providers, utility companies, and...
Read Blog
Learn How Florence eConsent will Simplify Your Consent Process
Request A DemoAccess a personalized on-demand tour of Florence eConsent
Take The TourFlorence eConsen: An Interview with Mason McLellan with CEDAR at OHSU Knight Cancer Institute sharing why their organization moved to eConsent, how they did it and the impact it’s making.
Watch Video
Florence eConsent: An Interview with Morgan Oats at Levine Cancer Center sharing why their organization moved to eConsent, how they did it and the impact it’s making.
Watch Video
By Andrea Bastek, PhD, Sr. Direction of Innovation at Florence and former Assoc. Director of Clinical Affairs for Abbott 82% of sponsors and 88% of research sites plan to have eConsent software...
Read Blog
Sites and sponsors struggled with clinical trial diversity long before the COVID-19 pandemic began. Roughly 20% of new drugs have different effects depending on a person’s race. This makes it...
Read Blog
By Rachelle Stover, MPH, CCMP With the start of a new year, both people and organizations begin thinking about change. Perhaps there’s a new technology or software your clinical trial organization...
Read Blog
89% of sponsors now embrace decentralized clinical trials (DCTs). With DCTs becoming commonplace, sites, sponsors and CROs have turned to the FDA for guidance on how to use clinical trial...
Read Blog
ICH E6(R2), the current global standard for good clinical practice (GCP), went through an update in 2016–and it’s already undergoing another major revision. With how quickly changes are happening,...
Read Blog
by Crystal Stargell, Associate Product Manager for Florence and former Clinical Regulatory Coordinator Informed consent is arguably the most important element of clinical research. It’s during the...
Read Blog
In November 2021, Florence hosted over 200 clinical research professionals at the first-ever Innovation Summit to discuss the latest trends in clinical trials. Going paperless was the most...
Read Blog
Access a personalized on-demand tour of the Florence eBinders platform
Take The TourRead Flipbook
Join Florence Chief Clinical Trial Officer, Catherine Gregor, to learn how to prepare your annual capital expenditure site budget for scalability.
Watch Video
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...
Read Blog
Join Ryan Jones (Florence CEO), Kat Meagley (Florence eConsent Product Manager), and Blake Adams (SVP Marketing Florence) to discuss how to streamline the move to eConsent.
Watch Video
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?” ...
Read Blog
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...
Read Blog
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...
Read Blog
Loading More...
