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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

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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.
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