How Sponsors & CROs can start-up and collaborate with “frontier” sites

Too Many Trials, Too Few CRAs - Maximizing CRA Efficiency

Breaking Down the FDA's 2022 Guidance on Diversity

Learn from Catherine Gregor about the newly published FDA draft guidance for increasing participant enrollment from underrepresented racial and ethnic groups in clinical trials.

Florence eConsent - An Interview with Mason McLellan at OHSU Knight Cancer Institute

Florence 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.

Florence eConsent - An Interview with Morgan Oates at Levine Cancer Institute

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.

Innovating Inclusive Study Startup and Recruitment | Florence Innovation Summit

This is a recording of our keynote panel during our Innovations Summit in Feb2022 discussing how the clinical research industry is innovating to focus on diversity and inclusion.

Digitizing the Site Network for Traditional and Decentralized Clinical Trials

Watch this panel discussion on digitizing the site network for traditional and decentralized clinical trials.

How to Prepare Your Annual Capital Expenditure Site Budget for Scalability

Join Florence Chief Clinical Trial Officer, Catherine Gregor, to learn how to prepare your annual capital expenditure site budget for scalability.

How to De-Risk Your Move to eConsent Webinar

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.

Florence Innovation Summit 2021

Listen to a recording from our first Innovation Summit in October of 2021 where we discuss with the Florence community of sites, sponsors, and CROs on how they are using innovative technology.

How to Scale Clinical Trials with Technology

Industry veteran, Rebecca Kush, PhD, Chief Scientific Officer of Elligo Health Research, explores the big picture of implementing and operationalizing key clinical research technology.

Florence Webinar - How to Maximize CRA Efficiency with an eTMF

How Research Sites Can Leverage a Purpose-Built eTMF and Why They Should

Where should you start if you are managing a multi-center study, grant-funded study, or Investigator-Initiated Trial in an eTMF? Find out in this complimentary webinar.

Decentralized Trials | Build the First Link to Site and Sponsor Connections

Decentralized trials isn't just a buzzword. Learn how this model will have a major impact on sites and clinical trial operations.

Moving Beyond COVID – The Sponsor and CRO Perspective on Lessons Learned

Hear from top clinical operations leaders, from the world’s largest pharma companies to a company transforming how CROs operate, to learn how they adjusted their processes and technology post-COVID.

Integrated Workflows: Empowering Your Day with Connected Tech

Moving Beyond COVID – The Site Perspective on Lessons Learned

Hear from clinical research operations leaders about how COVID impacted their operations, how they adjusted, and what lessons they will take with them as they speak to their optimism for the future.

Data Protection and Privacy in Clinical Trial Technology 101

This webinar is jam-packed with not only the basics of data privacy but practical takeaways and resources to help you walk the walk as regulations continue to take shape across the globe.

Avoiding Failure When Migrating to a New eTMF

Whether you’re considering an eTMF or want to ensure your strategy is effective, watch this webinar to learn how to successfully migrate to a new eTMF.