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    Breaking News

    SaaS Solution Introduced for Guided Compliance in Medtech Product Development

    Cognition Corporation's solution is designed to automate the product development process in compliance with industry standards.

    PR Newswire08.24.20
    Cognition Corporation, a developer of SaaS solutions for medical device and pharmaceutical product development, has launched Compass 2020. The new SaaS solution enables medical device product teams to automate and document the entire design control process—tightly integrating risk, requirement, and test management—with built-in quality processes. Compass guides development to support compliance with standards and regulations such as ISO 14971, FDA 21 CFR 820.30, and ISO 13485 to speed product development. 
     
    "For 20 years, Cognition has been building custom software implementations based on our Cockpit platform for the industry's largest medical device companies. Cockpit is optimized for large, complex projects where diverse data is interconnected and implementations are highly customized because requirements/SOPs are diverse. Compass is based on the proven and powerful Cockpit technology and provides a prepackaged, templated product for medium-sized companies that do not have the time, resources, budget, or need for a fully customized solution," explained Dale Gallaher, president of Cognition Corporation.
     
    Compass provides template-based guided compliance through the medical device product development process and enforces quality processes across every connection. In addition, it provides a single point of truth so that when changes are made, they are made everywhere and potential effects of the change on other data are flagged. Compass enables small and midsize medical device companies to bring products to market faster while supporting compliance with industry standards and regulations by combining automation with the most scalable trace matrices and most comprehensive risk management tools—all integrated with quality systems.
     
    "Before introducing Cockpit/Compass, Mediso used requirement management tools, which provided little support in defining our processes. With Cockpit/Compass and Cognition, we instantly gained access to document templates, workflows, and a knowledge base, which guided us to perform our processes in better compliance with critical standards and good engineering practices. We were able to upgrade existing processes based on what we learned from Cockpit/Compass, and at the same time these tools could be fine-tuned to areas where we already had solid foundations. We expect that this solution will help us to better manage our modular product family, and so accelerate time to market—enabling Mediso, a relatively small company, to compete with the industry giants," said Miklós Czeller, R&D director at Mediso, a medical diagnostics company.
     
    "Compass streamlines our product development processes, with complete confidence that we are in compliance with critical standards, by providing the needed templates to guide us in developing our LDT Software Platform. It provides a centralized environment for collaboration while ensuring that all data is correctly connected, with every activity and user action updated in real time across the process. Cognition's solution ensures teams spend significantly more time focused on productive work, rather than building and maintaining documents and complex traces. This allows us to run lean and still accelerate our time to market more than any other solution I've had experience with," said Chris W. Henry, senior manager, Software Quality Engineering at Epic Sciences, a medical diagnostics company.
     
    Key features of Compass include:
    • Integrated Risk Management: Industry-leading risk management techniques, optimized for the embedded design process, are tightly integrated with requirements and test management to provide real-time views of the impact of changes across the design process. 
    • Automated Design Controls: Step-by-step implementation of rigorous processes in design data and requirements management supports the creation of Design History File (DHF) content. 
    • Test Management: Clearly connects testing to requirements that are linked to risk mitigation, closing the loop for risk control, and implementation. 
    • Scalable Trace Matrices: Supports the largest, most complex traces—with master trace matrices in excess of 10,000 items—and traces are automatically generated and updated when any changes are made. 
    • Document Management: Integrates predesigned workflows for easy review, approval, and release with auditable sign-off. 
    • Project Management: Real-time visibility into the status, activities, and detail of every aspect of the project. 
    • Software Validation: Validation kit includes test execution results for Compass out-of-the-box functionality, based on AAMI TIR36 and GAMP 5 validation, and an optional validation services subscription plan to complete software validation based on specific use cases in your environment. 
     
    Compass has multiple use cases including speeding time to market, exiting remediation, creating Design History Files (DHF), and supporting compliance with standards and regulations like ISO 14971, 21 CFR 820.30, and ISO 13485. It provides real-time dashboards and connectors to popular tools like JIRA and GitHub. 
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    Related Buyers Guide Companies

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    • Heraeus Acquires Mo-Sci Corporation, ETS Technology Holdings

      Heraeus Acquires Mo-Sci Corporation, ETS Technology Holdings

      The two deals will strengthen Heraeus' healthcare and medtech portfolio.
      Heraeus 09.22.21

    • MedTech Innovator Names the Finalists for the Title of MedTech Innovator 2021

      MedTech Innovator Names the Finalists for the Title of MedTech Innovator 2021

      Attendees of The MedTech Conference, powered by AdvaMed, will vote for the Grand Prize winner.
      MedTech Innovator 09.21.21

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    CURRENT ISSUE

    September 2023

    • Superior Subtractive Solutions for Machining Medtech
    • Medical Device Industry Experts' Thought on Assembly & Automation
    • Power Trip: A Discussion of Custom Medical Electronics
    • The MDR Transition: An Opportunity for Design Change?
    • View More >

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