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THE RESULTS YOU NEED.
THE EXPERIENCE THEY DESERVE.


TECHNOLOGY TO CONNECT, INFORM, AND EMPOWER PATIENTS IN GLOBAL CLINICAL TRIALS.

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CONNECT

 * Site & Sponsor Hub
 * Trial Awareness
 * HCP Community Activation
 * Site Selection


INFORM

 * Consent Management
 * Education
 * eConsent | eSignature
 * Data Insights & Modeling


EMPOWER

 * Transportation Management
 * Med Adherence Monitoring
 * Participant & Caregiver Portal
 * eDiary & TeleVisit


RESOURCES

Previous
Guide

ADAPTIVE EXPERIENCES: 3 KEY CONSIDERATIONS FOR SUCCESSFUL IMPLEMENTATION

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Case Study

CONNECTING HCPS (AND THEIR PATIENTS) TO A PHASE 3 TRIAL FOR FRONTOTEMPORAL
DEMENTIA

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White Paper

CONSENT MANAGEMENT: MOVING BEYOND SIMPLE ECONSENT

Download White Paper
Guide

ADAPTIVE EXPERIENCES: 3 KEY CONSIDERATIONS FOR SUCCESSFUL IMPLEMENTATION

Download Guide
Case Study

CONNECTING HCPS (AND THEIR PATIENTS) TO A PHASE 3 TRIAL FOR FRONTOTEMPORAL
DEMENTIA

Download Case Study
White Paper

CONSENT MANAGEMENT: MOVING BEYOND SIMPLE ECONSENT

Download White Paper
Guide

ADAPTIVE EXPERIENCES: 3 KEY CONSIDERATIONS FOR SUCCESSFUL IMPLEMENTATION

Download Guide
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WHY CLINONE

With so many technology providers, we understand it can be overwhelming to know
whom to trust. ClinOne provides a true single platform built to be easily
configured for your protocol while making it easier for patients, caregivers,
and sites to actively participate in your trial. And our team is comprised of
seasoned leaders with decades of experience at the industry’s largest technology
providers.



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WHAT SETS US APART

Since 2016, ClinOne has supported sites, patients and caregivers in clinical
research with a single platform for HCP Trial Awareness, Consent Management, and
Patient Engagement.

TRUE SINGLE PLATFORM

FASTEST DEPLOYMENT IN THE INDUSTRY (2-8 WEEKS)

COST-EFFECTIVE AND CONFIGURABLE

100% ON-TIME IMPLEMENTATION

INTEROPERABLE WITH API AND WEBHOOKS

DEVELOPED IN COLLABORATION WITH SITES


TRUSTED PARTNERSHIP

Sponsors, CROs, and site networks of all sizes rely on ClinOne technology to
conduct their trials and improve the patient experience worldwide.




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STILL HAVE QUESTIONS?

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