ON-DEMAND WEBINAR The Florence Regulatory Pulse: Q3 2026 Regulatory guidance for clinical trials shifts every quarter, often before trial teams notice. The Florence Regulatory Pulse is a quarterly briefing for clinical operations, regulatory affairs, quality, and technology leaders who are responsible for keeping trials inspection ready. Each session covers the most [...]
ON-DEMAND WEBINAR Flo & Tell Roundtable: Been There, Passed That: Inspection Readiness Tips & Tricks Inspection readiness isn't something you scramble for two weeks out. The sites that walk into audits calm are the ones who built readiness into how they work every day, not the ones with the thickest binder. In [...]
ON-DEMAND WEBINAR Win More Studies, Not More Paperwork: A First Look at Site Feasibility Repetitive questions. Scattered spreadsheets. Missed SLAs. If feasibility questionnaires feel like reinventing the wheel every time, there's a better way with Florence Site Feasibility. In this webinar, you will learn: The biggest feasibility bottlenecks sites face today, from scattered tracking to re-entering the same info again and again (up to 80% of every questionnaire) How Florence Site Feasibility's AI-powered knowledge library surfaces your team's own vetted answers instantly, walled off by therapeutic area for accuracy Speakers Michael Wong, Sr. Product Manager - Site Feasibility, [...]
WEBINAR The Florence Regulatory Pulse: Q3 2026 Regulatory guidance for clinical trials shifts every quarter, often before trial teams notice. Florence Regulatory Pulse is a quarterly briefing for clinical operations, regulatory affairs, quality, and technology leaders who are responsible for keeping trials inspection ready. Each session covers the most consequential regulatory developments [...]
ON-DEMAND WEBINAR Flo & Tell Series: From Set-Up To Sign-Off, Best Practices for DOA and eLogs Join us for a practical, peer-driven conversation about eLogs and Delegation of Authority (DOA) logs. We'll explore how sites approach setup, maintenance, and day-to-day use - including strategies teams use to encourage adoption and make [...]
ON-DEMAND WEBINAR Scale Without Breaking: How HCA Healthcare Rolled Out eRegulatory Across 54 Sites in 21 States As one of the nation's largest multi-specialty research networks, HCA Healthcare recognized early that sustainable growth required modernized infrastructure. Rather than patch existing systems, they made the strategic decision to rebuild from the ground [...]
ON-DEMAND WEBINAR From Imaging Chaos to Clarity: How Yunu + Florence Streamline Clinical Trial Imaging for Sites, CROs and Sponsors Clinical trial imaging doesn’t have to be the part of your study that keeps you up at night. Join Florence Healthcare’s Chief Clinical Trial Officer, Catherine Gregor, along with technology partner [...]
ON-DEMAND WEBINAR The AI Inflection Point: 2026 State of Clinical Trial Technology Industry Perspectives Florence’s annual report is back, and we’re ready to share the results with you on February 17 at 11 a.m. ET. Join us as we share findings from a global survey of 400+ sites, sponsors, and CROs—and unpack what [...]
REGISTER NOW From Imaging Chaos to Clarity: How Yunu + Florence Streamline Clinical Trial Imaging for Sites, CROs and Sponsors February 26, 2026 11:00 a.m. CT Clinical trial imaging doesn't have to be the part of your study that keeps you up at night. Join Florence Healthcare's Chief Clinical Trial Officer, [...]
ON-DEMAND WEBINAR Flo and Tell Roundtable Series: ICH E6 (R3) and Computerized Systems Florence Healthcare's Sara Saunders and Elina Huttunen host the following peer discussion on what R3's computerized systems requirements mean for Florence users: from compliance expectations to practical workflows. Quick Highlights: Validation approaches that balance compliance with practical workflows [...]
ON-DEMAND WEBINAR Navigating the 'No AI' Clause Minefield: Best Practices for Clinical Trial and Research Agreement Negotiations As AI reshapes the world and R3 brings new rules about software in clinical trials, there has been a surge of “No AI” clauses in CDAs and clinical trial-related agreements. Many sites are finding [...]
ON-DEMAND WEBINAR Flo & Tell: User Community Roundtable Series Rewatch this interactive roundtable on eConsent best practices, where industry peers will share lessons learned, practical strategies, and creative approaches to improving the participant consent experience. Walk away with: Practical strategies to improve participant experience Tips for smoothing adoption and maintaining compliance [...]
ON-DEMAND WEBINAR The Future of Sponsor-Site Partnerships: ROI, Adoption, and Industry Change Sponsors are under pressure to accelerate enrollment, streamline operations, and prove ROI, all while navigating complex site needs and entrenched industry norms. Florence Healthcare and 1nHealth will share how their models empower sites and deliver measurable results for sponsors. [...]
ON-DEMAND WEBINAR Staffing for Efficiency & Expertise: How to Allocate Resources and Leverage Service Providers in Start Up Study startup remains one of the most complex, misunderstood, and resource-intensive stages of the clinical trial lifecycle. As protocols grow more intricate and timelines tighten, sites and sponsors alike face mounting pressure to [...]
ON-DEMAND WEBINAR R3 and Me: The Good, The Bad, and The Ugly R3 is here—and with it comes opportunity, complexity, and a lot of questions. In Part 2 of our ICH E6(R3) Demystified series, we’re moving beyond the basics and digging into the real-world implications of the updated guidance. R3 and [...]
ON-DEMAND WEBINAR ICH E6(R3) Demystified: What It Means for You As clinical trials evolve globally, the new ICH E6(R3) guidelines represent a critical shift for sponsors, sites, CROs, and vendors. In this on-demand webinar, clinical research professionals gained actionable insights into what ICH E6(R3) means for their day-to-day operations and long-term [...]
AI-Powered Contracting: Unlocking Speed and Precision in Clinical Trials
Navigating Post-Inauguration Shifts: The Dual Impact of Policy Changes and Government Funding Cuts on Clinical Trials
ON-DEMAND WEBINAR How Sponsor & CROs are Investing in Site-Facing Capabilities Unlocking Operational Gains and Site Adoption with the Right Tech Strategy Sponsors and CROs are rethinking their approach to site-facing technology—moving beyond disconnected tools to scalable, integrated solutions that truly support site operations. In this webinar, we dive into: Why [...]
ON-DEMAND WEBINAR How the eISF Has Changed and What You Need to Stay Ahead Your eISF/eRegulatory solution should be keeping up with your research. A lot has changed in the last few years of how an eISF can support your studies, and organizations are migrating systems without disrupting their operations. In [...]
ON-DEMAND WEBINAR Navigating Canadian eRegulations and Clinical Trials Landscape The regulatory landscape in Canada is changing—are you prepared? This webinar breaks down the latest updates in clinical trial compliance, privacy laws, and regulatory frameworks affecting sponsors, sites, and CROs. What you’ll learn: ✅ The impact of Quebec’s Law 25 and upcoming [...]
ON-DEMAND WEBINAR Navigating the Future of Technology Enabled Clinical Trials in 2025 Gain exclusive insights from Florence’s 2025 State of Technology-Enabled Clinical Trials report in this on-demand webinar. Whether you’re a sponsor, site, or CRO, this session is packed with actionable strategies to streamline workflows, enhance collaboration, and stay ahead in [...]
ON-DEMAND WEBINAR Remote Monitoring 101: Tips and Tricks for Streamlining Start-Up and Monitoring at Florence-Enabled Sites Discover how to optimize your workflows at Florence-enabled sites. With over 30,000 sites leveraging Florence eBinders as their electronic Investigator Site File (eISF), this on-demand webinar is your ultimate resource for boosting efficiency during start-up [...]
ON-DEMAND WEBINAR Simplifying Enrollment: Introducing Florence's New Enrollment Automation Solution for Research Sites Discover how eNcounter, Florence’s newest solution, automates and simplifies participant enrollment for research sites. Watch our on-demand webinar to learn how this platform improves recruitment efficiency, from automated pre-screening to real-time tracking, all while keeping participants engaged. In [...]
ON-DEMAND WEBINAR How Remote Monitoring and Document Automation Can Reduce Your Site Management Costs Staying ahead in clinical trials means getting smarter about how we handle our operations. In this webinar, Florence's CEO, Ryan Jones, dives into how leveraging remote monitoring solutions and document automation can reduce your site management costs by 25.7%. [...]
ON-DEMAND WEBINAR The Power of Site Enablement for Streamlined CRO-Site Collaboration: Insights from the 2024 CRA Monitoring Report Uncover the game-changing impact of remote site monitoring and electronic Investigator Site Files (eISF) on Clinical Research Associates (CRAs) and the wider industry. This session provides a comprehensive analysis of our biennial benchmark [...]
ON-DEMAND WEBINAR Strategic Vendor Relationships for CROs: A Playbook for Optimizing Operational & Financial Performance In the competitive world of clinical research, strategic vendor relationships can be the key to optimizing your operations and maximizing ROI. Join Florence Healthcare and industry experts for a compelling webinar that explores how CROs can [...]
ON-DEMAND WEBINAR What You Need to Know in 2024 for Global Clinical Trial Compliance Tune in to Florence compliance expert, Sara Saunders as she examines US FDA 21 CFR Part 11 and its EU counterpart, Annex 11. Uncovering the foundational requirements for utilizing electronic records and signatures in the US and the [...]
ON-DEMAND WEBINAR Executive Insights: A Technology Roadmap for Clinical Trial Sponsors to Build Better Site Connectivity Are you confident every site is ready for an unexpected inspection? Are all of their documents accurate and ready for closeout and submission to the TMF? Join Florence Site Enablement experts, Keith Wright (Director of [...]
ON-DEMAND WEBINAR Critical Strategies for Sponsors and CROs in 2024: Measuring Site Enablement Maturity This webinar explores five key areas of site enablement that are crucial for building relationships with sites, ensuring adequate participation in studies and ensuring the success of research. Attendees will leave with practical, actionable strategies that can make [...]
The State of Clinical Trial Technology in 2024 Ryan Jones, Catherine Gregor, and Blake Adams, explore the critical insights from the much-anticipated 2024 State of Tech-Enabled Clinical Trials report. They dive into the evolving landscape of Site Enablement, focusing on the need for genuine site-centric strategies in clinical trial [...]
ON-DEMAND WEBINAR Unlocking Efficiency with VersaTrial: Your Essential Tool for Simplifying Study Operations Are you tired of juggling countless documents, passwords, and sponsor contacts to manage your studies? Discover how the VersaTrial Study Organizer, a cutting-edge, free, and easy-to-use tool, is transforming the way research sites streamline their study management. Designed for clinical [...]
ON-DEMAND WEBINAR Going Digital: Overcoming Sponsor Resistance to Change Are paper forms and manual processes holding back your clinical research? Are you feeling the burden of capacity issues and inefficiency? Is your sponsor not as excited about transitioning from paper to digital processes? Don't let outdated methods slow you down! Watch this webinar [...]
ON-DEMAND WEBINAR Debunked: Myths and Misconceptions About eConsent Adoption Say goodbye to paperwork woes and hello to the future of streamlined processes! The digital revolution is reshaping the landscape, and we’re here to unravel the mysteries behind the lingering hesitation toward digitizing informed consent. Ready to dive in? In this webinar, you [...]
Transforming Clinical Trial Sites with Technology: An Optimized Approach to Delivery and Adoption Gain first-hand insights from industry experts on maximizing site adoption and success, including Keith Wright (Director of Site Enablement at Florence Healthcare), Lauren Perrey-Moore (Clinical Research Manager at Indiana University School of Medicine, Neurology), Matthew Wheeler (Managing Director at L.E.K. [...]
On-Demand: Site Enablement, Partnerships, and Integrations in Clinical Trials During our Q2 Innovation Summit we brought together clinical trial site executives, technology experts, and industry leaders to discuss the latest advancements in site technology and collaboration. Throughout this session we: Had a panel discussions featuring site users sharing their experiences with site [...]
How to Embrace Technology at Sites and Drive Change with Florence's Approach to Site Enablement Missed the live webinar? No problem! You can still access our recorded webinar on "How to Embrace Technology at Sites and Drive Change with the Florence Site Enablement Playbook." Discover the power of going digital and learn from [...]
On Demand: The Clinical Trial Technology Landscape Missed the live event? No worries! You can still access our recorded Florence Innovation Summit on the Clinical Trial Technology Landscape, available now on-demand. Join our expert panel as they take a deep dive into the various categories, vendors, and interactions available in the clinical trial [...]
On-Demand Webinar: How To Avoid Clinical Trial Technology Pitfalls Missed the live webinar? No problem! You can still access our recorded webinar on "How to Avoid Clinical Trial Technology Pitfalls." Join our expert speakers, including Catherine Gregor, Chief Clinical Trial Officer, Nardin Farid, Solutions Engineer, and Kristin Surdam, Senior Director, KOL & Strategy, [...]
On-Demand Webinar - What You Need to Know from the 2023 State of Clinical Trial Technology Report Missed the live webinar? No problem! You can still gain valuable insights into how 450 of your fellow clinical research leaders plan to invest in technology this year by watching our recorded webinar. During this informative [...]
On-Demand Webinar: Why Linking Tech in European Clinical Research Studies is Critical for 2023 Missed the live webinar? Don't worry! You can still gain valuable insights into the latest trends in clinical research by watching our on-demand recording of "How Technology is Driving Innovation in Europe." Join our expert panel for a discussion [...]
Research Revolution 2022 Recording: Successfully Implementing New Technology Did you miss the live panel discussion at Research Revolution 2022 on successfully implementing technology across the enterprise? No problem, you can still access the on-demand recording and learn from industry experts on how to implement technology successfully. Listen to the following expert speaker provide [...]
Panel Recording from Research Revolution 2022: What does it mean to be a sponsor of choice? In this panel session from Research Revolution 2022, our expert speakers provide a comprehensive discussion on what it takes to be a clinical trial sponsor of choice. You'll gain valuable insights into the key factors that sites [...]
Research Revolution 2022 Sessions: From Traditional to Digital Site Collaboration Missed the live session at Research Revolution 2022 on standardizing site collaboration with a Site Enablement Platform? No worries, you can still access the on-demand recording and learn from industry experts. Speakers Include: Ryan Jones, CEO of Florence Healthcare Dr. Christina Brennan, Senior [...]
Watch: Moving Beyond COVID - The Sponsor and CRO Perspective on Lessons Learned Hear from a panel of top clinical operations leaders from the world's largest pharma companies, like Pfizer, to a company transforming how CROs operate to learn how they adjusted their people, processes, and technology; and what lessons [...]
Watch: Avoiding Failure When Migrating to a New eTMF In theory, the Trial Master File (TMF) is a collection of documentation that tells a cohesive story. But all too often sponsors are left piecing this story together retroactively due to disjointed site and sponsor systems, outsourced TMF management, and traditional [...]
Watch: Moving Beyond COVID - The Site Perspective on Lessons Learned Hear from clinical research operations leaders at Vanderbilt Ingram Cancer Center, AdventHealth, and MultiCare about how COVID impacted their operations, how they adjusted their team and technology, and what lessons they will take with them as they speak to [...]
Watch: Data Protection and Privacy in Clinical Trial Technology 101 Data Protection and Privacy is a critical component of what you do every day as a clinical research professional, but are you confident in your knowledge? Or does the threat of non-compliance keep you awake at night? This webinar will [...]
Watch: 2021 State of Clinical Trial Technology Industry Report Hear the latest insights, trends, and analysis of how clinical trial operations are shifting heading into 2021. After the most disruptive year in clinical operations, several new innovative solutions arrived on the scene. Remote Site Monitoring, Remote Source Verification, eConsent, Decentralized [...]
Watch: Global Remote Clinical Trial Site Access for Monitoring and Source Data Review Remote access to your study sites is now a requirement for continuing effective clinical operations. While COVID forced sponsors and CROs to pivot to remote site access, over 80% of sponsors and sites indicate they expect most [...]
Recording: Florence eLogs Inside Look Learn How to Remove the Paper Log Bottleneck at Your Research Site Let’s face it, paper logs are not only antiquated, they are holding you back from reaching higher levels of accuracy, output and collaboration at a time when innovation and ingenuity are central to continuing to [...]
Watch: Florence and VirTrial Present the Future of Remote Site Access and Virtual Site Monitoring The current research landscape is transforming rapidly and evolving your operations to remote workflows is a must-do to survive and thrive. Have you seen the need to drastically change the way your organization operates over [...]
Watch: Remote Monitoring 101 - Setting Your Site Up for Success with MAGI Learn how you can equip your research site to participate in the remote transformation as clinical trial operations shift to remote monitoring, SDV, start-up, and management. In this recorded webinar learn what your research needs to be equipped [...]
Watch: Eliminate Clinical Trial Bottlenecks with Advanced eISF Workflows Discover how over 7,200 research sites around the world are eliminating common bottlenecks in their research operations by harnessing the #1 eISF platform. In this on-demand webinar learn how organizations like Levine Cancer Institute are harnessing Florence to automate and streamline workflows [...]
Watch: Capabilities of a Modern eTMF Discover what capabilities your eTMF must have to streamline operations for the modern clinical trial. It is critical that you have the right eTMF to maximize your operations in a rapidly shifting clinical trial environment. More than ever, your eTMF will either be an essential [...]
Webinar Recording On-Demand Webinar: Busting eRegulatory Myths In this recorded webinar you will hear how clinical research leaders overcame key reasons their teams, PIs, and Sponsors were resistant eRegulatory platforms. What you will learn: How to get buy-in from your Principal [...]
Florence Recorded Webinar: eISF Reference Model Overview Download eISF Reference Model Florence eBinders eISF Power your research operations by moving your Investigator Site File to the eISF Standard - Florence eBinders. Over 6,200 active sites trust our intuitive platform to help them accelerate research. [...]
On-Demand Webinar: Successful Change Management in Clinical Research Discover the secrets to building a change management plan that ensures technology adoption in clinical research and clinical trials. Watch Now Why watch? Purchasing the right software solution for your research site is only half the battle. The other half – and [...]
Webinar Recording: Solving eTMF Quality and Completeness How Sponsors and CROs are solving the weakest link in Trial Master File Completeness and Quality - site document access. Admit it, eTMF inspection readiness keeps you up at night. In this webinar, learn from your peers about how to fix it with a [...]
Watch: 2020 State of the Industry Webinar Discover how it is now possible to directly integrate the eTMF and the Research Site eISF to accelerate research by connecting in a unified digital ecosystem. As you prepare for 2020, it is essential to ensure you are focusing on the right priorities, especially [...]
Watch: eRegulatory: One Year Later Listen to this recording of our guest panel of clinical trial site representatives discussing the realities of implementing an eRegulatory solution. During this webinar research organizations like Moffitt Cancer Center and the University of Arizona Cancer Center shared first-hand stories of implementing eRegulatory including: What benefits [...]
Watch: eTMF + eISF Integration - Why and Why Now? Discover how it is now possible to directly integrate the eTMF and the Research Site eISF to accelerate research by connecting in a unified digital ecosystem. The use of electronic documentation in clinical trials, both at the site (eISF) and the [...]
Webinar Recording: Best Practices for Managing Multicenter Research As the number of multicenter trials continues to grow, it is essential that coordinating centers begin thinking about their technology like a sponsor. This is especially important when it comes to the management of your data and documents. Leading coordinating centers are now [...]
Watch: Best Practices for Multicenter Research Management with Technology Learn best practices, tips, and tricks for managing multicenter clinical trials with technology. Multicenter research introduces unique challenges and bottlenecks for clinical trial leaders who are expected to manage studies across sites. To avoid study delays and compliance risks when managing multi-site [...]
Recorded Webinar: Investigator eRegulatory Adoption and Training Best Practices How do you convince your investigators to adopt electronic systems like eRegulatory and eSource, and then train them to use it effectively? When considering eRegulatory/eSource solutions, failing to properly prepare for successfully migrating and training investigators will, at best, delay your project - [...]
Watch: Remote Monitoring 101 Webinar Is your team prepared for the increasing shift to remote monitoring and oversight? Leading research teams are getting ahead of sponsor and CRO demands by establishing their remote monitoring strategies now that harness this shift to optimize their operations. View this recorded Florence webinar to learn: [...]
