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 * Workflows
     
   * * For Sponsors + CROs
       * * Remote Site Start-up – Remotely deploy electronic study binders and
           workflows to study sites globally.
         * Remote Site Monitoring – Activate always-on, remote monitoring of
           study sites electronic Investigator Site Files.
         * Remote SDR + SDV – Conduct remote source data review and verification
           of site subject binders.
         * Electronic Trial Master File – Streamline trial master file workflows
           on a flexible and site connected platform.
         * Electronic Consent – Deploy patient-centric electronic informed
           consent workflows to study sites.
     * For Research Sites
       * * Electronic Investigator Site Files – Streamline site regulatory
           documents and administrative workflows on the electronic Investigator
           Site File.
         * Electronic Participant Binders – Simplify source collection, storage,
           management and remote access with electronic participant binders.
         * Electronic Consent – Enable electronic consent workflows for for
           participants in an easy-to-use interface.
         * Electronic Logs – Eliminate paper logs and complex systems from your
           workflows with custom electronic logs.
         * Multi-Site Management – Manage multi-site and multi-location trials
           with digital document and administrative workflows.
     
 * Products
   * * SiteLink – Always-on, Remote Workflows with Your Sites
     * eBinders – Electronic Binder Workflows for Sites
     * eConsent – Electronic Consent Workflows
     * eTMF – Electronic Trial Master File Workflows
 * Industries
   * * Large Sponsors – How Florence helps large sponsors build global
       workflows.
     * Large CROs – How Florence helps large CROs build global workflows.
     * Emerging and Midsize Sponsors – How Florence helps emerging and midsize
       sponsors scale their operations.
     * Emerging and Midsize CROs – How Florence helps emerging and midsize CROs
       scale their operations.
   * * Research Sites – How Florence helps research site organizations.
     * Site Networks – How Florence helps Site Networks, IITs, and
       Multi-Location Trials
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     * Certifications
       * * Digital Research Certification – Learn the fundamentals of digital
           clinical trials and get certified by Florence.
         * Change Management Certification – Learn how to drive change at your
           organization and get certified by Florence.
     * Essential Info
       * * FDA Guidance – Resources for understanding FDA guidance on technology
           in clinical trials.
         * CFR Part 11 – Resources for understanding FDA Title 21 CFR Part-11
           compliance.
         * ICH GCP R2 – Resources for understanding ICH GCP E6 R2.
         * GDPR Guidance – Resources for understanding GDPR guidance on clinical
           trials.
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         * Guide to eRegulatory – Guide to moving to electronic regulatory
           workflows.
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           solutions.
     
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     * Compliance – Understand how Florence support global compliance.
 * Schedule my demo


Florence Healthcare | Goodbye Chaotic Clinical Trial Workflows. Hello
Florence.Blake Adams2022-08-17T13:53:16-04:00

GOODBYE CHAOTIC WORKFLOWS.
HELLO FLORENCE.

Streamline clinical trial workflows with electronic documents and always-on,
remote site-sponsor links.


See Products
Schedule Demo


Research Revolution Conference


INDUSTRY SPONSORS

Accelerate study timelines and increase site satisfaction by linking to your
study sites for remote, continuous workflows.

Large Sponsors
Emerging + Midsize Sponsors

CROS

Hit milestones faster and maximize your workforce efficiency by remotely linking
to your sites and your sponsors.

Large CROs
Small + Midsize CROs

RESEARCH SITES

Simplify and integrate workflows across studies, teams, and multi-site locations
and activate remote access for sponsors.

Research Sites
Site Networks


WHY TRUST FLORENCE FOR YOUR CLINICAL TRIAL WORKFLOWS



REMOTELY LINKS SITES AND SPONSORS

Always-on, remote digital document and administrative workflows transform the
way sponsors, CROs and sites work together in traditional site-based and
decentralized trials.



MAKES SITE STAFF HAPPIER

Study sites rate Florence #1 for ease of use, setup, and support. If you’re a
site leader giving your team eBinders or a sponsor/CRO deploying eBinders to
your sites, you can count on them loving it.



MAXIMIZES EMPLOYEE PRODUCTIVITY

Linked workflows improve employee efficiency and productivity. Reduce the impact
of hiring and retention challenges. CRAs on Florence can monitor 60+ sites per
week.



EXPANDS PATIENT ACCESS

Remote links with study sites in historically underserved areas increase access
to diverse participant populations. Florence’s network of 10,000 connected study
sites is already within 25 miles of 80% of the US population and in 45 countries
worldwide.



ACCELERATES STUDY TIMELINES

Standardizing processes while still enabling flexibility to adapt to individual
site processes helps increase efficiency and accelerate timelines. Florence’s
solutions reduce study start-up times by 40% in most instances.



INCREASES SAFETY AND COMPLIANCE

Audit trails, version controls, controlled user access, and built-in PHI
redaction take the risk out of going digital. Adverse events workflows and
electronic consenting coupled with real-time remote site monitoring improve
participant safety.

Florence’s platform is helping Pfizer to respond to the changing environment due
to COVID-19 and further progress COVID-19 research with the capability to
perform remote monitoring where approved by regulatory authorities and ethics
committees.

Rob Goodwin
VP and Head of Operations in Global Product Development
Pfizer




ACCORDING TO USER REVIEWS, FLORENCE IS RATED THE #1 CLINICAL TRIAL WORKFLOWS
PLATFORM FOR EASE-OF-SETUP, EASE-OF-USE AND CUSTOMER SUPPORT.



WHY BEING RATED #1 OUT OF 190 CLINICAL TRIAL PLATFORMS ON G2, THE PEER-TO-PEER
REVIEW SITE, MATTERS FOR YOU.

 * High Adoption: We lead the industry with 92%+ site technology activation per
   study.

 * Faster Timelines: Intuitive workflows that eliminate duplicate work mean work
   gets done fast.

 * Low FTE Burden: You don’t need large dedicated IT teams to support
   implementation and management.

 * Always Reliable: Our customers have had 100% uptime over the last 12 months.
   We’re there when you need us.



Read More Customer Reviews




IN CLINICAL RESEARCH, COMPLIANCE IS CRUCIAL. WE’VE GOT YOU COVERED.









FLORENCE’S RESEARCH WORKFLOW PRODUCTS


SITELINK™

Activate always-on, remote workflows with study sites.

 * Remote Site Start-up

 * Remote Site Monitoring

 * Remote Source Data Review

 * Remote Source Data Verification

 * Electronic Investigator Site Files


Learn More


EBINDERS™

Simplify administrative and operational workflows across your site.

 * Electronic Investigator Site Files

 * Electronic Participant Binders

 * Electronic Logs

 * Multi-location Management

 * Remote Monitoring


Learn More


ETMF

Standardize your trial master file and connect to sites through SiteLink.

 * Standard TMF Structures

 * Document Routing Workflows

 * Connection to Sites with SiteLink

 * Submittal and Archiving

 * Flexible and Scalable Platform


Learn more


ECONSENT

Simplify informed consent workflows with participants.

 * Similar to Paper Workflows for Ease-of-use

 * Intuitive Interface for Participants

 * Automatic Version Controls

 * Compliant eSignatures from Anywhere

 * Standardized Consent Across Sites and Studies


Learn more

“Our eTMF QA score went from a 65% submission pass rate to 98.7% by having
real-time remote access to the site eISF.”

Aperio Clinical Outcomes

“92% of 140 study sites in 8 countries were activated on Florence for remote
source access and monitoring in four weeks.”

VP Clin Ops, Top 3 Pharma

“Our highest performing CRAs are now ‘visiting’ 64 sites per week with remote
monitoring on Florence, up from 2 per week.”

VP Clin Ops, Top 3 Global CRO


FLORENCE SUPPORTS REMOTE WORKFLOWS ON A GLOBAL SCALE

Florence now supports workflows between sponsors and more than 10,000 study
sites in 45 countries.




WE ARE COMMITTED TO MAKING YOU AND YOUR SITES SUCCESSFUL.

0%
Site Adoption Rate
0%
Uptime Past 12 Months
0min
Avg. Support Response Time

We love working with sponsors on Florence. Collaborating in real-time on a
single document management platform helps us tackle study tasks faster and keep
research on track.

Dr. Christina Brennan
VP of Clinical Research




LATEST RESOURCES + NEWS

Press Release

FLORENCE EBINDERS EARNS LEADER BADGE IN G2’S FALL 2022 REPORTS

Blog Post

HOW TECHNOLOGY CAN EMPOWER CAR T-CELL THERAPY CLINICAL TRIALS

Blog Post

FLORENCE SUPPORTS DIVERSITY IN CLINICAL TRIALS THROUGH A PARTNERSHIP WITH THE
MEHARRY-VANDERBILT ALLIANCE




GET STARTED


Schedule Demo
2022 Industry Report


INDUSTRIES

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 * Large Sponsors
 * Large CROs
 * Emerging + Midsize Sponsors
 * Emerging + Midsize CROs
 * Research Sites
 * Site Networks

COMPANY

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 * Careers
 * Florence News
 * Upcoming Events
 * Leadership Team

GET IN TOUCH

Schedule my Demo
info@florencehc.com
Join Email List


PRODUCTS

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 * SiteLink
 * eBinders
 * eTMF
 * eConsent

LEGAL

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 * Privacy
 * Terms of Use

GLOBAL OFFICES

USA (HQ)
600 Peachtree St. NE, Suite 920
Atlanta, GA 30308

--------------------------------------------------------------------------------

Serbia
Bulevar Kralja Aleksandra 84
11000 Belgrade, Serbia



© 2022. Florence Healthcare.





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