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LiveWorx 2018
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s802 - Using Integrity to Build Requirements Management Capability in the Medical Device Industry

Session Description

Johnson & Johnson Medical Devices, like many competitors, is facing an environment that includes shifts in technology to include more modular and software-enabled systems, increasing Regulatory requirements that products must meet, and increasing pressure to drive product development to a faster timeline. All of this adds up to increasing complex products that must be initially designed and updated throughout their time on the market. One of the ways J&J Medical Devices is meeting this challenge is to not only deliver product innovation but to also innovate the tools and practices our teams follow to realize high quality and more efficient product development. Embracing Systems Engineering practices is a key enabler for us to realize faster, more robust product engineering. A primary way we are meeting this challenge is to leverage the power of Integrity as our tool for practicing Requirements and Risk Management in a systematic, data-centric manner.

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Product Design & Business Process
Requirements Management
Learn how Johnson & Johnson used Integrity Lifecycle manager to increase product development efficiency.
Get an in-depth overview of the importance of properly managing requirements.
Learn how to overcome regulatory burdens.
Breakout Session
45 minutes
Session Schedule
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