Manufacturers find it challenging to produce products efficiently and keep a competitive edge as medical devices get more complicated and regulatory oversight strengthens. There are, however, constant ways to increase compliance while still advancing innovation, market-access speed, and data quality.
Product Lifecycle Management (PLM) for Medical Devices is an integrated end-to-end system for product development that uses reuse, context capture, and collaboration to address complexity and regulation. Medical device producers can save costs and compliance risks while increasing the visibility and traceability of their products’ competitively differentiating devices.