Visit the Autodesk web site
Click on the advert above to visit the company web site

Product category: PLM and collaboration software
News Release from: Dassault Systemes | Subject: Enovia MatrixOne
Edited by the Engineeringtalk Editorial Team on 11 July 2006

Enhanced PLM for the medical device
industry

Request your FREE weekly copy of the Engineeringtalk email newsletter. News about PLM and collaboration software and more every issue. Click here for details.

PLM accelerator drives profitability, collaboration and compliance at each stage of the product lifecycle

Dassault Systemes (DS), a world leader in 3D and Product Lifecycle Management (PLM) solutions, has announced the latest updates to the MatrixOne Medical Device Accelerator (MDA) The MatrixOne MDA manages Quality System Regulation (QSR)/ISO-regulated design processes, projects, documents and data, and is the only medical device-tailored solution built on an enterprise-class PLM platform that has been proven effective at the industry's top three device manufacturers

Being innovative and responsive in a regulated environment is complex and requires enterprise collaboration, control and coordination.

While innovation and change are the lifeblood of successful medical device companies, they often get bogged down in administrative regulation details, losing sight of customer needs along with piling up resource inefficiencies.

The MatrixOne MDA is designed to meet the specific needs of medical device manufacturers.

"The MatrixOne Medical Device Accelerator is allowing Possis to better manage the entire product development process," said Tim Anderson, director of engineering, Possis Medical.

"Giving everyone on a project team access to information - including RandD, quality, engineering, design, marketing, production, regulatory affairs, and senior management - will make Possis a more collaborative and efficient organisation".

The MDA's features are subdivided into three major groups: Enterprise Design Control, which provides configurable templates and workflows to streamline the product design process; Documentation and Change Control, a central repository for documents and data; and Project and Program Control, enabling a collaborative environment for managing projects, design activities, drive process standards and provide enterprise visibility.

Other noteworthy features include: exploit Integration to Microsoft Office tools to manage documents "Medical device companies are under increasing pressure to speed time-to-market while needing to meet stringent regulatory demands," said Barry Foster, medical devices product director for Enovia MatrixOne.

"We understand the needs of medical device manufacturers and have created a product that will allow them to work in the type of environment that they are used to, while improving innovation, accelerating product development, and meeting federal regulations".

Dassault Systemes: contact details and other news
Email this article to a colleague
Register for the free Engineeringtalk email newsletter
Engineeringtalk Home Page

Search the Pro-Talk network of sites

Visit the Autodesk web site