Save Time and Reduce Risks Throughout the Medical Device R&D Lifecycle

The Trusted, Quicker Path from R&D to FDA Submission

Access flexible, intelligent design control solutions for the entire medical device development lifecycle. Compass® MED is a medical device R&D management software solution that helps MedTech teams unlock greater engineering efficiency, fewer regulatory risks, and more reliable data management.

Unlock Efficiencies

Automate complex processes that are critical for medical device regulatory compliance, and stay on track with aggressive FDA submission timelines.

Manage Risk at Every Step

Easily generate risk management plans, product risk analyses, and more.

Strengthen Your Data Management

Change once, update everywhere functionality delivers more reliable data throughout the product development lifecycle.

Ready to Reduce Your Medical Device’s Time-to-Market?

Fill out the form to schedule a conversation with the Cognition team, and discover how the Compass MED platform expedites medical device product development.

Unlock Efficiencies Across the Product Development Lifecycle

With built-in workflows, customizable workspaces, compliance templates, and more, Compass MED supports MedTech R&D and Systems Engineering teams throughout the full medical device product development lifecycle.

Requirements Management

Compass MED links risk items with requirement items for verification of implementation, giving MedTech teams a powerful tool for requirements management.

Risk Traceability

Compass MED tightly integrates risk management in the design control process from the very start of product development to drastically reduce manual upkeep.

FDA Submission Management

Accelerate your medical device’s path to market with submission-ready documentation, generated with the click of a button.

Regulatory Compliance and Audit Readiness

Users can easily access properly formatted, QMS- and regulatory-compliant documents, reports, and traces for their own use and use downstream.

Real Results with Compass MED

Compass MED has helped leading medical device teams accelerate the path to market with more efficient R&D workflows.

“Compass MED provides unprecedented visibility and control, helping us proactively identify and address issues before they escalate.”

“Compass MED helps us run lean and still accelerate our time to market.”

“Compass MED gives us clear traceability to ensure appropriate verification and validation. You don’t get that with spreadsheets and word docs.”

“Compass MED helps us overcome the increasing burden on medical device manufacturers to meet standards and regulations.”

“We used to manually create data and maintain connections in paper DHFs. With Compass MED, we can maintain large trace matrices much easier.”

Power Your Medical Device R&D

Get a conversation with the Cognition team on the calendar and accelerate your path to submission.