Unleash Your Products with
Real World Evidence

Capture Data for a Purpose

Leverage PatientIQ to partner with leading academic physicians & researchers to collect scientific data on your full product range.

Comprehensive Multicenter Registries

PatientIQ’s HIPAA compliant, cloud-based platform is perfect for hosting outcomes registries.  Our team of experts can guide you through designing your trial, drafting the protocol, IRB regulatory approvals, post-market surveillance requirements, and launching a high-quality research project that will answer important clinical questions.

Leading Academic Physicians are Already Collecting Outcomes Data on Our Platform

PatientIQ was designed to seamlessly integrate with the busy day-to-day workflow of a physician. Research data collection is no longer a hassle, but rather an opportunity for physicians and industry to work together to improve the innovation landscape in healthcare.

Real-time Analytics to Inform your Product Strategy

The era of paper data collection instruments is long gone. Watch in real-time as data is uploaded to the PatientIQ platform from anywhere in the world and get instantaneous access to comprehensive analytics.

Create Studies to Demonstrate How Your Product is Better than the Competition

Design a comprehensive device registry or prospective research trial that measures clinical, device, and patient-reported outcomes over time. Use our automated statistical analysis and data visualization tools to make your data actionable.

Real World Evidence powered by pIQ

Electronic Data Capture

Systemically collect data across your investigational sites and monitor case report forms in real-time from our cloud-based platform.

FDA Compliant eSignatures

eConsent subjects electronically on any device. Our electronic signatures are compliant with the FDA’s CFR Part 11 Title 21 standards.

Patient Reported Outcomes

Painlessly collect validated PRO instruments and custom data elements directly from the patient.

Data Driven Insights

Leverage our statistics-decision engine and cohort analysis tools for regulatory submissions, publishing research, and internal product development.

FDA Guidance on RWE

Our EDC platform complies with the FDA’s Guidance on RWE and is optimally suited for capturing real world data on your entire product portfolio.

IRB Consultation Services

Our team of experts can assist with drafting your protocol & other essential study documents, regulatory submissions, site data monitoring, and performing advanced statistical modeling.

Ready to start?

Together let’s transform your organization into a data-driven enterprise. Leave the heavy lifting to us.