Siemens product lifecycle management (PLM) Software for life sciences can help medical device manufacturers manage compliance requirements while supporting greater collaboration, ultimately reducing costs while improving patient outcomes. Deployed properly, Siemens PLM Software can deliver payback in less than a year. Siemens PLM Software for life sciences provides support for end-to-end product lifecycle management and collaboration on a common platform. Key capabilities that support medical devices manufacturers include:
Teamcenter is a single source of product and process data that supports automatic device master record (DMR) creation, linking, maintenance, and validation against Federal Drug Administration (FDA) guidelines; device history record (DHR) creation, validation, and revision; and support for integrated corrective and preventive action (CAPA) complaint tracking, related workflows, and reporting.
NX supports design and styling requirements, visualization, real-time and photorealistic rendering, and digital simulation.
Tecnomatix supports manufacturing planning and simulation so that factors that affect cost, quality and productivity can be evaluated virtually so changes to product and production designs can be made early in the process.
Siemens PLM Software enables manufacturers to systematically manage regulatory compliance with end-to-end traceability and reporting while providing authorized outside parties with the ability to access and provide input.