Get Connected
6 cards
Resources on Florence Healthcare's community and engagement offerings, including events, certifications, customer programs, and networking opportunities like FloPro training and The League.
Research Revolution – The Event of Clinical Research
The Research Revolution Summit is a premier event focused on the latest advancements and innovations in clinical research. It brings together industry leaders, researchers, and professionals to share insights and foster collaboration in the field.
FloPro - Professional Training and Certifications
Get FloPro™ Certified on Florence's Products. Advance your career with a FloPro Certification! Beyond just bragging rights, this certification validates your expertise in Florence’s products and unlocks new opportunities within your organization and industry.
Join the League: Powered by Florence
Join The League, an invite-only group of senior executives from sites, sponsors, and CROs who are advancing cures through technology.
FlorenceCare™ - Florence
FlorenceCare™ is a service designed to prioritize customer needs in the healthcare sector. With a strong foundation since 2014, it connects clinical teams across 90+ countries and boasts impressive customer service metrics.
Clinical Research Events and Webinars | Florence
Register and learn all about events, webinars, and courses related to the clinical research industry. Stay updated on the latest opportunities to enhance your knowledge and network within the field.
Florence Announces Model Context Protocol Access
Florence Healthcare announces the release of Model Context Protocol (MCP) access for its entire application suite. This new feature enhances the capabilities of their platform, providing users with improved access to protocol management tools.
Essential Information
8 cards
Key resources on clinical trial compliance, including FDA guidance, GDPR, HIPAA, and ICH GCP E6 (R3) requirements.
Privacy, Data Protection, and Compliance | Florence
When it comes to data protection, Florence’s commitment to personal data privacy and security goes above and beyond.
Library of FDA Guidance for Electronic Document Management
The Florence library of the FDA's responses to GCP inquiries regarding electronic processes in clinical investigations, like ICH guidelines for case report forms and FDA guidance on wet ink signatures.
Compliance, A Shared Responsibility Model - Florence
Compliance is a shared responsibility between Florence and our customers. Florence interprets the technical and procedural requirements of applicable global regulations so that our customers can have time back in their day to focus on research.
21 CFR Part 11 - FDA Requirements for Electronic Records
Guidance on FDA Title 21 CFR Part 11 regulations for electronic documentation and electronic signatures and how it impacts Clinical Trials.
ICH GCP E6 (R3) Good Clinical Practice Guidelines
ICH GCP E6 R3 guidelines outlining the significant implications for clinical trial sponsor and site technology and document management.
GDPR and Clinical Trials: Impact, Resources, and Q&A
Learn what you need to know about GDPR and clinical trials. All information is sourced from official GDPR documentation and outlined in an easy-to-use format.
Guides
12 cards
A curated of guides and eBooks on clinical trial site enablement, covering eRegulatory, eTMF, eISF, compliance, and site management topics.
Top 5 Strategic Imperatives for Clinical Leaders in 2026
Read the top five strategic imperatives for clinical leaders from Florence's annual State of Clinical Trial Technology Report. This resource highlights key trends and insights essential for effective leadership in clinical settings.
How Sponsors Can Ensure Their Sites Are Aligned with ICH E6 R3
Explore how sponsors can support clinical trial sites in meeting ICH E6(R3) requirements—from system validation to data governance, remote monitoring, and updated site agreements.
Practical Considerations for eRegulatory Adoption in Canada
As Canadian sites, sponsors, and CROs increasingly adopt eRegulatory solutions, the country aims to enhance transparency and efficiency in clinical trials. This guide will examine best practices for choosing the best systems to assess their effectiveness and impact in clinical trials.
The Complete Guide to Enrollment Automation Platforms for Sites - Florence
Discover how enrollment automation platforms streamline participant enrollment for sites, covering core features, ROI metrics, and more in this free guide.
Site Enablement Spotlight: Connecting the eTMF and eISF
Boost your eTMF strategy with our expert guide. Discover how tech advancements forge direct eTMF-eISF links, accelerating timelines and reducing risk.
How to Reduce Costs Across the Study Lifecycle
Discover how Florence’s Site Enablement Platform can streamline clinical trial operations and reduce costs by 25.7% with automated workflows and real-time document management.