Florence Healthcare

As a former Research Administrator at a federally-funded NCI Comprehensive Cancer Center, I am deeply concerned about the potential long-term impacts of the proposed changes to NIH funding. Federal support plays a crucial role in upholding essential infrastructure and fostering innovation. At Florence Healthcare, we stand firm in our dedication to assisting our academic partners amidst this period of uncertainty. Hence, we are providing our eISF services at no cost to all federally-funded studies, irrespective of their customer status. Our track record with federally-funded studies speaks volumes about our values. Florence, driven by a strong mission, has a longstanding practice of granting our enterprise site customers complimentary access to eBinders for their NIH-funded projects. This commitment now extends beyond our customer network to encompass a broader spectrum of grant-funded research initiatives. https://lnkd.in/eXJV79sb

Don't miss out! Join Andrea Bastek, Collier Wright, and Peter Brown from TruTechnologies, makers of TruLab, tomorrow at 11 AM ET for an exclusive webinar where they'll guide you through how to transition to digital workflows without disrupting your site operations! Learn how to: • Go paperless and balance hybrid workflows without slowing down your team • Use adaptable solutions to make your digital transition smoother • Leverage remote monitoring tools to stay inspection-ready, reduce site burden, and focus on what matters most: patient care • Invest in flexible, step-by-step approaches that lead to long-term success in clinical trials Save your spot: https://hubs.li/Q036rscZ0

This week's NIH+ funding disruption puts progress at risk and we won't take it lying down. Today we're making Florence's basic eISF available to all federally funded studies—whether or not your organization is a Florence enterprise customer. Our history with federally-funded studies: Florence is a mission-driven organization and since our start we’ve offered our enterprise site customers no-cost access to eBinders for their NIH funded studies. Now our commitment to grant-funded research extends to those outside of our customer base. We'll be sending an email out to our site list, but go here or DM me if we can help: https://lnkd.in/ey_jBijf

A Note from our CEO The potential disruption of NIH funding adds complexity to an already challenging trial landscape. To ensure research continues uninterrupted, we are extending free access to Florence’s basic Electronic Investigator Site File (eISF) for all federally funded studies—whether or not your organization is a Florence enterprise customer. Our history with federally funded studies: Florence is a mission-driven organization and since our start we’ve offered our enterprise site customers no-cost access to eBinders for their NIH funded studies. And now our commitment to grant-funded research remains as strong as ever. If your institution is navigating uncertainty, we’re here to help maintain the critical infrastructure that keeps your research on track. Get started for free or reach out to our team for more information. Let’s keep critical research running—together! 🔗 https://hubs.li/Q036ppZM0

The 2025 SCOPE Summit brought together the brightest minds in clinical research to discuss what’s next for our industry. From policy shifts to AI-driven innovation, one thing is clear: clinical trials are evolving fast and staying ahead means adapting now. Here are five key insights every clinical trial leader should be tracking according to Florence CCTO Catherine Gregor: ‣ Policy changes are on the horizon: The industry is bracing for regulatory shifts that could reshape trial operations. ‣ Bringing research to the community remains a priority: But making decentralized trials work requires more than just good intentions. ‣ The push for data standards and interoperability is stronger than ever: Sites need better tech alignment, and sponsors are taking notice. ‣ New trial and site models are proving effective: Hybrid and virtual trials are showing real benefits, but scaling them requires strategic oversight. ‣ AI is the hot topic—but will it deliver? Sponsors are investing, but the industry is still determining which AI applications will drive lasting impact. The future of clinical trials demands smarter site orchestration—ensuring sites, sponsors, and technology work in sync. #SCOPE2025

Meet up with Florence during the Clinical Trials Innovation Programme at the Clinical Trials Conclave (CTC)! 🔹 Looking to streamline your clinical trial operations? 🔹 Want to explore how Florence can help accelerate site connectivity? Join Simon Taylor at Booth 8 to discuss how Florence’s site-first technology empowers research teams to work smarter and faster or book 1:1 time with him here: https://hubs.li/Q035_tL_0 #FlorenceHealthcare #ClinicalResearch #CTIP2025 #ClinicalTrialsInnovation #SiteEnablement

Paper is still prevalent in clinical trials, especially for source documentation. But going digital isn’t just about reducing site burden—it’s also about giving sponsors clearer oversight into trial progress and compliance. Join us on February 13 at 11 AM ET / 8 AM PT for a live webinar with Florence Healthcare on how sponsors can help sites transition to digital workflows—without disrupting operations. 📅 Save your spot: https://lnkd.in/e_UVpz8s

Clinical trials are facing increasing challenges with more studies and fewer staff paired with high turnover and manual burdens from paper documents. The pressure is real. But it doesn’t have to be this way. Join Andrea Bastek (Florence Healthcare) and Collier Wright and Peter Brown (TruTechnologies, makers of TruLab) on February 13 at 11 AM EST as they discuss how to: • Reduce the burden of paper and manual workflows • Optimize document management with seamless digital solutions • Simplify onsite monitoring visits keeping your sites inspection-ready while reducing on-site burdens. Save your spot: https://hubs.ly/Q035CkbZ0

Choosing the right Content Services Platform (CSP) for clinical research isn’t just about technology, it’s about ensuring compliance, security, and scalability. Our latest capability checklist breaks down the key factors you should evaluate in your RFP process, including: ✅ Regulatory Compliance: FDA 21 CFR Part 11, HIPAA, GDPR, ISO 13485 🔐 Security & Document Management: Encryption, audit trails, automated workflows 🌍 Integration & Scalability: API support, interoperability, and global deployment 📊 Vendor Expertise: ROI transparency, cost efficiency, and implementation support 💡 Get the full checklist to streamline your vendor evaluation and make informed decisions: https://hubs.li/Q035t4Xv0

4,700+ sites. 49% more capacity. $2M cost savings per study. A leading global CRO partnered with Florence Healthcare to scale operations while reducing CRA workload and travel costs. With remote monitoring, automated workflows, and seamless site collaboration, they transformed efficiency—without adding more staff. Want to see the impact for yourself? Read the case study now: https://hubs.li/Q0354XLD0