Manufacturers that make custom devices must move beyond conventional engineering practices to an automated and collaborative engineer-to-order process.
CAPA provides visibility into critical product quality characteristics, failures/ non-conformances, and resolutions to these issues for smarter decisions across the global, extended enterprise. With the right solution, design, manufacturing and quality improvement teams can share the same views of the information they need to directly impact Six Sigma and Lean initiatives.
How can medical device companies establish end-to-end regulatory compliance as a strategic initiative?
Traditionally, PLM vendors had come to the market with a very heavy product focus and then customers really had to adapt and understand how that product functionality mapped into their particular industry and their industry processes. Siemens’ new Industry Catalyst Series aims to augment its products so that customers can get there faster. An interview with the Mad Scientist behind the series.