Real-World Evidence (RWE) Solution

A better way to collect primary real-world data (RWD) for RWE studies.

Create engaging patient experiences that improve study participation and efficiency with an easy-to-use and powerful platform. Pattern’s platform powers clinical trials and RWE studies, including support for hybrid and decentralized trials. We make it easy to collect data, including biometrics and eCOA, and support integration with third-party data sources such as RWD service providers and electronic health record (EHR) systems.

Pattern powers RWE studies of all varieties, including:

○ Long-term follow-up studies

○ Observational studies

○ Post-authorization safety and efficacy studies (PASS)

○ Registries

Prototype in as little as 48 hours.

Adopted by 350+ research sites.

Serving 800K+ end users.

More Smart Technology.
Less Costly Services.

Pattern’s easy-to-use clinical trial solution is available in self-serve and managed service models. We combine our expertise and technology to deliver a unique solution, including:

✔ Rapid study setup using no-code tools.

✔ Library of integrated devices and industry services.

✔ Flexible implementation options.

✔ Automated workflows reduce study team burden.

✔ User experience patients and study teams love.

A Better Way to Manage RWE Studies

Pattern supports trial designs of all varieties, from site-based to hybrid and fully decentralized. Our unified platform is built to power studies from end to end and can interoperate with any existing eConsent, eCOA, EDC, and EHR vendors.

Implement Protocol Design
No-code Configuration
eCOA Library
Activity Library

Screening
eConsent
Enrollment
Education
Telehealth Screening

Connected Devices
eCOA
Engagement
Televisit
Educational materials
Activity tracking
Notifications & Reminders
Communication
Medication Adherence

Automated Workflows
Site & Study Team Apps
APIs
Real-Time Analytics
Cloud Infrastructure

PARTICIPANT EXPERIENCE

Reduce patient burden and boost retention with engaging experiences

Eligibility Screening

Access broader populations & identify suitable participants. Deploy pre-screening questionnaires to filter inclusion/exclusion criteria.

eConsent

Seamlessly obtain informed consent. Our electronic records and signatures are 21 CFR Part 11 compliant.

Communication

Engage with participants 1:1 and in groups through in-app messaging as well as email and text.

Onboarding

Introduce participants to your study and app. Improve retention and engagement through early education.

eCOAs & ePROs

Use surveys to collect patient outcome data. 100+ commonly-used COAs & PROs pre-built.

Connected Devices

Capture biometric data from devices, sensors, and wearables. Existing integration and flexibility to support your preferences.

Educational Content

Engage and inform participants with information about your study over text and video.

Adherence Framework

Personalize and engage at scale using an automated, data-driven approach. Customize experiences based on eCOA results, biometric data, and more.