We hit the ground running with a fully validated set of templates that matched our product development process.
Bedford, Massachusetts (PRWEB) August 14, 2013
The Cognition Lifeline Program is designed specifically for use in small companies, especially for ones that sell medical devices. It comes with the Cockpit Validation Kit to help ensure regulatory compliance. This product is powerful for companies looking for an easy way to meet regulatory standards without spending a lot of time and effort.
Cognition's team members all have years of senior level experience in medical device compliance. If any company is starting out and unsure of what the best way to ensure compliance is, Cognition will provide them with industry standard document formats to start them off on the right track with Market Requirements, Product Requirements, Design Inputs, Process, and Software Requirements. It also includes FMEA, Hazard Analysis, and Fault Tree Analysis. Test protocol templates are also built in. The company will have its own complete system containing all their product development documents on the web.
According to Dan Kussman of BSC, “The Cognition Lifeline Team worked with our organization to prepare the appropriate documents and traces for our project. We hit the ground running with a fully validated set of templates that matched our product development process.”
Cognition can host the Lifeline or it can be hosted internally. Contact us to set up a one hour web session to introduce Cognition’s Product Development Lifeline Program.
Cognition Corporation, based in Bedford, Massachusetts, has been offering solutions for product and process development for more than ten years. Cognition offers two core products: Cognition Cockpit™ and Enterprise Cost Management™ (ECM). Thousands of users worldwide have used Cockpit and ECM to manage their product development and to meet performance, cost, risk, and schedule targets.