Worldwide
Worldwide
Français
日本語
中文
Deutsch
Русский
DS Norden
Español
Italiano
ENOVIA for the Industries
Relentless global competition and increasing product complexity are pressuring manufacturers across industries to extract more time and cost improvements from their development teams and business partners. Whether you are creating airplanes, cars, cruise vessels, nuclear power plants, consumer goods or apparel, you need a flexible collaboration environment for managing your global product development processes. Leveraging your intellectual assets and industry best practices, ENOVIA can help you take to market higher-quality products faster and manage them from conception to end-of-life.
Downloads
- NEW! Whitepaper - Automate Contract Manufacturing with PLM
- NEW! Whitepaper - Bridging the Gap Between Compliance and Innovation: ENOVIA V6 Solutions for Life Sciences
- Backgrounder - How PLM Provides a Competitive Advantage for LS Companies
- Whitepaper - Streamlining Quality Assurance and Regulatory Compliance in the Life Sciences Industry
Life Sciences companies of all sizes face a competitive marketplace where it is vital to deliver innovative new products while ensuring compliance with increasingly stringent federal regulations that govern every aspect of design and manufacturing. To continually deliver successful new products to market, companies need to drive innovation throughout entire new product development lifecycle, streamline business processes and improve collaboration between globally distributed design, development and manufacturing teams.
By combining years of Life Sciences industry experience with best-in-class collaborative business processes, ENOVIA PLM solutions provide companies with the tools they need to ensure a successful, FDA and ISO compliant product rollout. Whether you are in the medical device or another life sciences product development industry, ENOVIA combined with our industry specific solutions can help you to streamline business processes and reduce new product development time through one cohesive source of information that allows management and collaboration of design information and visibility into every product development process.
ENOVIA Life Sciences Accelerator™ for Change Control
ENOVIA Life Sciences Accelerator™ for Engineering Design
ENOVIA Life Sciences Accelerator™ for Quality Issues
ENOVIA Life Sciences Accelerator™ for Stage Gate
“PLM improves productivity and optimizes regulatory compliance for us. The[ENOVIA] technology is a big step in our corporate strategy for growing business and introducing innovative life-saving products
Dozens of Life Sciences and pharmaceutical companies worldwide including Abbott, Medtronic, Philips Medical and more depend on ENOVIA to:
- Speed compliance with FDA regulations including Title 21 CFR Part 11, which prescribes the accepted use of electronic records and signatures in medical device manufacturing
- Achieve cost and time savings through efficient re-use of Intellectual Property (IP).
- Reduce overall engineering time through one cohesive solution that allows management and collaboration of design information and visibility into the complete product development process.
- Improve global new product introduction processes to drive profitable growth through cycle time reduction and increased resource productivity
- Consolidate supply base and develop strategic suppliers and partners
- Emphasizes process definition - improve common enterprise processes, then track and measure those processes as a basis for improvement