hello@patientrials.com

RESEARCHERS & CLINICIANS


Streamline your operations to manage multiple studies across sponsors with an unified interface and empower patients with self-care in clinical trials.
PatienTrials unleashes the barriers for patients to participate in clinical trials. Our proprietary software is the first to bring clinical trials on to a HIPAA & GDPR compliant instant messaging platform.
As a high enrolling clinical research site, managing and keeping up with multiple patients with regulatory and accountability documents can be time consuming. Additionally common tasks of patient follow up and treatment reminders can take away valuable time of your site coordinators. Allow PatienTrials to do the routine tasks of reaching out to all study members for their appointment and treatment reminders without clinicians interactions. Empower patients by enabling them on our platform to increase patient engagement, patient compliance and patient retention. Not only they can reach out to study nurse and doctors, they can also converse with auto agent supported by proprietary artificial intelligence. With PatienTrials analytics dashboards, you can develop engagement strategies to increase retention rates in your site. Get instant patient engagement statistics to proactively identify potential dropouts, so that resources can be directed towards them to retain, optimizing site operations increasing overall productivity.
  • Self service site solution
  • Single platform for all your studies
  • eConsent and Re-Consent
  • Study specific Surveys
  • Site searchable by sponsors
  • Patient recruitment deep link
  • Shortlist patients based on rules
  • Shorter study timelines
  • Reduce Study Risk
  • High Quality Data
Optimize your site operations with PatienTrials solutions
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Site level community to enhance patient adherence.
  • Treatment information at patient finger tips
  • Instant visibility to patient adherence
  • Access to study staff and resources
  • Personalized AI agent to track Medications and appointments
  • Video conferencing with study staff at pre-arranged times
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Interactive informed consent & Re-consent
  • Pre-screening
  • Onboarding
  • Schedule surveys for collecting timely data
  • Randomize certain surveys for better response
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Manage multiple studies, site structure, resources and compliance from a single platform.
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AI (Artificial Intelligence) agent monitoring for adverse events and responding to study services requested by subjects/patients.
FOLLOW US
Patient Centric Platform for Clinical Trials.
EMAIL ID
hello@patientrials.com
CONTACT US
PatienTrials Inc
WeWork Legacy West
7700 Windrose,
Plano, TX 75024,
USA.
PatienTrials Inc
MATTER
222 Merchandise Mart Plaza,
Suite 1230,
Chicago, IL 60654
USA.
PatienTrials Inc
#176, 4th Floor,
Adarsh Eco Place,
KIADB EPIP 2nd phase, Whitefield,
Bengaluru, Karnataka 560066,
India.
© Copyright 2018 - PatienTrials, a company of PatienTrials Inc.