Cognition Compass MED
Why Choose Cognition Compass MED?
You should choose this if you’re a medical device company looking for a ready-to-go solution that keeps your product development compliant and organized. It saves you time with built-in templates and automates complex workflows, making regulatory stuff less painful.
Compass is a pre-configured, out-of-the-box, SaaS solution purpose-built to connect data across all functional areas of medical device product development, leveraging regulations such as 21 CFR 820.30 as well as standards ISO 13485, IEC 62366, and ISO 14971 as the foundation of the software design. It enables compliant product development by ensuring the process of authoring, reviewing, and releasing is enforced via workflows and built-in document templates, and automates a complex workflow between those interconnections to ensure compliant development. It provides an adaptable set of document templates for the entire product design control process from user needs to validation, with a focus on risk, requirement, and test management. Saving time and resources, it maintains documentation and supports submissions as well as provides automatic generation of the master trace matrices and documents for the Design History File (DHF), Technical Documentation Records, or audit support. Compass is best suited for small- to medium-sized medical device companies looking for guidance on how to bring their products to market with less risk. Compass offers guided compliance that is fully functional out of the box.
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Cognition Compass MED Introduction
What is Cognition Compass MED?
Compass MED by Cognition Corporation is an intelligent design control solution for all your medical device development needs - including multi-level requirements, comprehensive risk management, and test management. Specifically engineered for medical device manufacturers and contract design organizations, Compass MED increases efficiency and enhances data integrity with real-time traceability, work instructions that accommodate guided compliance templates, regulation references with submission-ready documents, change once, update everywhere functionality, and more.
How to use Cognition Compass MED?
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Why Choose Cognition Compass MED?
You should choose this if you’re a medical device company looking for a ready-to-go solution that keeps your product development compliant and organized. It saves you time with built-in templates and automates complex workflows, making regulatory stuff less painful.
Cognition Compass MED Features
Administration
- ✓Requirements Listing
- ✓Centralized Information
- ✓Traceability
Communication
- ✓Stakeholder Communication
- ✓Internal Communication Enablement
Pricing
Standard
- ✓ Purpose-built for Medical Device Industry
- ✓ Integrated Requiements, Risk, and Test Management
- ✓ Reusable Libraries
- ✓ Document Centric and Data Centric Work Environments
- ✓ Built-In Processes to Meet Standards and Regulations
- ✓ Submission-Ready Exports
- ✓ Best-In-Class Customer Service
About Cognition Compass MED
What Is Cognition Compass MED?
Compass MED by Cognition Corporation is an intelligent design control solution for all your medical device development needs - including multi-level requirements, comprehensive risk management, and test management. Specifically engineered for medical device manufacturers and contract design organizations, Compass MED increases efficiency and enhances data integrity with real-time traceability, work instructions that accommodate guided compliance templates, regulation references with submission-ready documents, change once, update everywhere functionality, and more.