SaaS Solutions for Life Sciences Product Development and Regulatory Success
Unlock the full potential of product development with Cognition’s 20+ years of leadership in medtech and biopharma, and pioneering solutions for combination products.
Streamline Workflows. Ensure Regulatory Readiness. Empower Your Data.
Solutions by Industry
MedTech
Navigate regulatory speed bumps and accelerate the path to market for medical devices.
Combo Products
Take control of risk and untangle the complexities of bringing combination products to market.
BioPharma
Streamline drug development data pipeline, effortlessly manage complex datasets, and ensure regulatory compliance.
Streamlined SaaS Solutions for Biopharma and Medtech
Bringing life sciences products to market doesn’t have to feel like a series of speedbumps. Cognition’s out-of-the-box solutions offer a quicker path to the marketplace with structured data, traceability, and submission-ready documentation.
Compass® BIO
Transform your CMC processes with Compass BIO, a robust structured content and data management system for the complete biopharma product development lifecycle.
Compass® MED
Take greater control of medical device development with Compass MED, a structured data and design control SaaS solution purpose-built for medtech.
Compass® PRO
Navigate the complexity of combination product risk with ease with Compass PRO, a holistic risk management solution for your drug and device components.
More Efficiency. Less Risk. Quicker Time to Market.
See how to accelerate and elevate product development at every step with support from Cognition.
Insights from Cognition
See the latest events, market reports, customer stories, white papers, and more from the thought leaders at Cognition.

Webinar On Demand: Designing for Safety – How to Build Safer, More Usable Medical Devices
Medical devices are becoming more complex, more connected, and increasingly used in home settings by people with varying levels of technical skill. Designing for safety isn’t just good practice—it’s a regulatory and ethical imperative.

Webinar On Demand: From Concept to Compliance – Navigating Risk and Regulatory Submissions Across the Life Sciences
If you missed our recent panel discussion, “From Concept to Compliance: Navigating Risk and Regulatory Submissions Across the Life Sciences,” the full recording is now available to watch on demand.

Supercharge Your CMC Strategy with Structured Content & Data Management (SCDM)
In today’s data-intensive biopharma landscape, traditional content creation just can’t keep up. Discover how a Structured Content & Data Management (SCDM) approach to product development streamlines report generation, feeds AI/ML tools, and ensures submission-ready accuracy.

Webinar On Demand: Designing for Safety – How to Build Safer, More Usable Medical Devices
Medical devices are becoming more complex, more connected, and increasingly used in home settings by people with varying levels of technical skill. Designing for safety isn’t just good practice—it’s a regulatory and ethical imperative.

Webinar On Demand: From Concept to Compliance – Navigating Risk and Regulatory Submissions Across the Life Sciences
If you missed our recent panel discussion, “From Concept to Compliance: Navigating Risk and Regulatory Submissions Across the Life Sciences,” the full recording is now available to watch on demand.
Cognition: The Trusted Partner for Streamlined, Structured Submissions
Bringing products to market quicker, with less risk and greater efficiency; that’s the goal for any life sciences company. But with complex data being manually managed on pen and paper or spreadsheets, it can seem out of reach.
For the leading names in medtech and biopharma, Cognition makes that reality happen every day. With 20+ years of industry leadership and pioneering new solutions for combination products, Cognition transforms product development with greater efficiency, reduced risks, and an accelerated time to market.