For over 30 years, KMC Systems, Inc. has partnered with leading and emerging medical device companies to successfully bring in-vitro diagnostic, surgical, therapeutic, life science and laboratory automation instrumentation to market. The KMC Total Product Lifecycle Management Program provides customers with an experienced workforce of medical device design and manufacturing engineers, test technicians, supply chain experts and quality compliance specialists who turn smart ideas into brilliant reality.
The KMC360 development process leverages our depth of expertise and demonstrated success record. Through open communication and collaboration with our customers, our systems engineering team evaluates concept feasibility and architecture requirements with simulation tools in a virtual prototype environment to reduce development risk before investing resources in product design.
Our industry-recognized design team is made up of mechanical, electrical, software and systems engineers who are ready to solve your complex medical device design and engineering challenges. We provide design services for full instruments, from initial concept to production, and major instrument subsystems as well as enhancements to existing instrumentation and engineering support.
The KMC360 Manufacturing Execution System (MES) utilizes lean manufacturing methods, proven process management techniques, with workflow software for strict quality compliance. Applying these methods throughout every step of the process ensures lower manufacturing costs and accelerated time to market as well as compliance with FDA and ISO 13485 requirements.
Our partnership does not end when your product goes to market. As part of the complete suite of services the KMC360 Program provides premium depot-level service to support medical instrumentation including repair and refurbishment, spare parts management, logistics, service manuals and documentation creation as well as field service engineer training.