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Medical Device

ENOVIA MatrixOne's expertise in the medical device industry is the result of our work with some of the most well-respected medical device companies, including the World's top three medical device manufacturers. Today, this expertise is being leveraged by medical device manufacturers of all sizes as they are being challenged to speed product innovation to market while ensuring compliance with increasingly stringent federal regulations.

MatrixOne Medical Device Accelerator for Regulatory Compliance
ENOVIA MatrixOne offers the Medical Device Accelerator for Regulatory Compliance to help companies manage complex, regulated business processes quickly and efficiently.

The MatrixOne Medical Device Accelerator for Regulatory Compliance is a comprehensive product lifecycle management (PLM) solution that manages your Quality System Regulation (QSR) and ISO-regulated design processes, projects, documents and data. It is built on top of Matrix10, the industry's most flexible PLM environment and enables medical device manufacturers to deliver market-leading products, drive responsive execution and achieve lean quality and compliance.

Medical Device Accelerator for Regulatory Compliance data sheet

Learn more

White Paper:

Streamlining Quality Assurance and Regulatory Compliance
in the Medical Device Industry: From Innovation to Execution

Recent Coverage:

Case Studies:
  • Possis Medical
    Possis implements ENOVIA MatrixOne product lifecycle management (PLM) solutions to manage product-related information.

  • Datex-Ohmeda
    Supplied and implemented by Sweden-based solution provider Technia, the ENOVIA MatrixOne product collaboration solution gives design, manufacturing and purchasing teams the right information at the right time.

  • MDS SCIEX
    The ENOVIA MatrixOne solution automates processes and manages information enabling product design and development teams to share evolving modules with each other in real time across multiple projects while also supporting quality control.

  • Medtronic Physio-Control
    The ENOVIA MatrixOne solution gives employees and suppliers access to relevant information early in the product development cycle, to save time and product development costs as well as ensure FDA compliance.

  • Smith & Nephew
    The ENOVIA MatrixOne product collaboration solution enables globally distributed design and manufacturing teams to have online, real-time access to BOM data, change processes, viewing tools, and the MRP system.

  • Terumo Cardiovascular Systems
    The ENOVIA MatrixOne solution enables the company to manage the device master record that encompasses the entire definition of the product, its manufacturing methods, and its release processes, showing the full history of the design.


Upcoming
Live Webcast:


Streamline Your Business, Improve Quality & Compliance in the Medical Device Industry

Thurs., March 22, 2007
2:00pm ET

Learn more & register »
highlighted Customer


Possis

Possis implements ENOVIA MatrixOne product lifecycle management (PLM) solutions to manage product-related information. Learn more...


Medical Device
Customers
Abbott
Calypso
Datex-Ohmeda
Elekta
eV3
GE Healthcare
Hospira
J&J Biosense Webster
J&J Cordis
J&J Ethicon
J&J ASP (Advanced Sterilization Products)
J&J LifeScan
J&J OCD (Ortho-Clinical Diagnostics)
J&J Therakos
JEOL
Kodak Health Group
MDS Sciex
MEDRAD
Medtronic
Packard Bioscience
PerkinElmer
Phillips Medical
Possis
Smith+Nephew
Sunrise Medical
Terumo
Toshiba Medical Systems
ev3
Quote: "The ENOVIA MatrixOne PLM solution … enables us to leverage a framework of best practices and to establish a solid, scaleable foundation for rapid business growth. In addition, as our company grows globally, ENOVIA MatrixOne’s solutions will enable us to stay compliant with multiple regulatory bodies in North America, Europe and the Far East, a key requirement of our business."

Pete Schaubach
CIO
ev3

up

Information: FDA 21 CFR