OVERVIEW

Complete eCOA solutions for clinical trials of all sizes

Clario’s enhanced eCOA study build, driven by science, delivers rapid setup and deployment to help meet critical deadlines through:

Simplified design specification review

Greater configuration

Faster translations

Pre-built, validated standardized assessment libraries

Clario’s vast experience in eCOA services includes:

  • 25 years of DCT and hybrid trials
  • A truly global scale with studies in over 120 countries and over 100 languages
  • Flexible technology options, including bring-your-own-device (BYOD), web or provisioned device
  • Configurable platform adapts to your trial needs

FREE ESTIMATION TOOL

Understand the starting cost of using paper PROs

With paper, you could be paying more for less.

See if paper is draining your budget.

Before your next trial, use our paper-cost calculator to estimate the potential starting expense of your patient-reported outcomes (PROs).

Flexible device modalities

Familiar devices, streamlined experience

Empower patients to participate in trials from anywhere using their smartphones or tablets, simplifying data collection and leading to faster enrollment. Clario’s secure platform ensures the highest quality data, giving you the insights you need for successful drug differentiation, development and regulatory approval.

example provisioned device iphone for eCOA data collection

Provisioned devices

example tablet for eCOA data collection

Tablets

BYOD iphone example phone screen for eCOA data collection

BYOD

example home computer for eCOA data collection

Home computer

Connected devices with eCOA

Make taking part in clinical studies straightforward

Clario’s devices are pre-validated for use in clinical trials and integrated with the eCOA device to capture date ECG, spirometry, blood glucose levels, activity levels, movement endpoints and many more.

Alivecor KardiaMobile6L

Go Spiro®

Glucometer

Opal® Precision Motion Monitoring

Ametris Watch

Ultrasonic Sensor

ACCESSIBILITY

Enhance participant accessibility for ePRO data collection

Ensure a seamless ePRO data collection experience for all participants with thoughtfully designed features that enhance usability and accommodate diverse needs.

ACCESSIBILITY FEATURE

Zoom In/Zoom Out

  • Increase accessibility:
    Include individuals with visual impairments who have a difficult time completing assessments.
  • Reduce bias:
    Minimize the need for caregiver assistance.
  • Reduce burden:
    Eliminate the need to remember reading aids.
  • Collect high-quality data:
    Extensively tested, science-led design that demonstrates equivalency and ensures all answer options are visible to participants.
  • Support improved compliance:
    Provide a better participant user experience.

ACCESSIBILITY FEATURE

Dark mode

  • Improved participant choice:
    A better user experience with the ability to choose between dark mode and light mode.
  • Reduced sensitivity to light:
    For individuals prone to conditions like migraines, bright screens can be a significant trigger.
  • Enhanced readability:
    Providing a higher contrast between the text and the background.
  • Reduced eye strain:
    Dark mode is designed to be easier on the eyes, particularly in low-light conditions.
Dark mode functionality Phone mockup

TEAM

Scientific guidance and therapeutic area solutions

Engage with our eCOA scientific and therapeutic area experts early on in your clinical development program to ensure the right eCOA endpoints are being measured, using the most appropriate assessments and the right technology. Our team has developed tailored solutions across multiple therapeutic areas and indications built upon 25 years of industry experience.

Our therapeutic area expertise across 560 indications

Endocrinology Icon

Endocrinology

Women's Health Icon

Women’s Health

Talk to a specialist

Our team of experts is available to address questions you may have about our integrated eCOA solutions. Submit your contact information and we’ll be in touch shortly.