Industry Summary Articles

As modern medical devices increase in complexity, manufacturers must ensure their products retain high quality and safety standards. Integrating engineering practices into the product lifecycle can help make this possible. In this free webinar, learn how to tame the behavior of “systems of systems” in medical device manufacturing.

Medical device manufacturers are struggling to manage the ever-increasing complexity of modern products. They have become systems – sometimes even systems of systems – whose product designs require a mix of hardware, software, electronics and/or firmware. Managing the system view of a product has traditionally been done with relatively simple tools, such as Excel, Access, PowerPoint, etc. That simplicity disappears when managing the behavior of “systems of systems”.

To succeed and win against sophisticated competitors, companies must excel at “the business of engineering in medical device manufacturing”, by verifying their system’s behavior and design as products progress through definition, development and the complete post-manufacturing product lifecycle. Otherwise, product quality issues will emerge, putting brands, companies, and their stakeholders at risk.

This webinar addresses the way in which robust system behavioral modeling can be integrated with downstream design practices to produce better, safer products. It is intended, through discussion of the latest advancements in system-level thinking, to help inform senior engineering professionals responsible for the cross-discipline lifecycle of their products.

Join Slavko Jovanovic, CEO & Partner at Minerva USA and Thomas Skogen, Product Director at Minerva Group in a live session on Friday, May 31, 2019 at 2pm EDT to learn more. This webinar will appeal to directors and other senior managers working in Engineering, Quality, Design, Regulatory and Development.

To view the original press release, and for more information or to register for this event, please click here.

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