Increase revenue and customer satisvation by integrating our platform into your service offerings.
Accelerate study builds with a modern platform and no-code tools.
Site-friendly technology improves site activation timelines, adoption rates, and satisfaction.
Unified capabilities include eConsent, eCOA, televisits, participant engagement, connected devices, and more.
Workflow automation improves study performance and reduces costs.
Interoperable with your existing solution providers, including eCOA, EDC, and others.
Pattern delivers speed and savings with a unified platform that scales to support your customer portfolio. We delivers something rare in our industry—easy-to-use technology and happy customers. Our platform offers no-code tools, configurable automation rules, robust clinical trial features, and user experiences study teams and patients love, available in self-serve and manage-service models.
Prototype in as little as 48 hours.
800K+ end users, 350+ sites.
Loved by patients and sites.
Speed and savings,
built to scale.
Pattern’s flexible architecture supports a wide array of use cases and is built to scale for global CROs. Join the movement that includes hundreds of organizations and over 800K users!
Global Clinical Trial Compliance
Pattern’s platform is trusted by biopharma, CRO, and academic customers to conduct clinical studies of all kinds, from single-site research to global phase IV clinical trials. We implement and maintain industry-standard measures that ensure regulatory compliance, secure and quality data, and privacy.Compliance at Pattern
Self-Serve or Let Us Handle Everything
Our easy-to-use, no-code configuration tools enable rapid study setup whether implemented by our experienced services team or an organization’s internal resources. CROs leverage our self-serve model to incorporate Pattern into their service offering.Enterprise Service Options
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