Medical Facilities

Medical Device Manufacturing, from Design to Commercialization

As a medical product manufacturer, you require fast turnaround of high-quality medical devices and components end users and patients can depend on. When you partner with Phillips-Medisize, you align with a world-class provider of medical device and combination product manufacturing services from design to commercialization. 

Phillips-Medisize is FDA registered and compliant to 21 CFR 820 and 21 CFR 210/211 for drug packaging and drug handling for drug coating application. You also benefit from: 

• Ongoing investment in state-of-the-art technology and equipment
• Flexible, secured work cells
• A culture of strict confidentiality
• Onsite collaboration areas for customers
• Pilot and clinical testing capabilities
• Automation to drive down costs and deliver high part repeatability
• Gowning procedures, Class 7 and Class 8 clean rooms
• Full services, from design to commercialization
• Low- and high-volume manufacturing capabilities
• Dedicated, onsite engineers with market-specific experience

Phillips-Medisize will handle your program with the dedication, pace, quality and confidentiality that meets your needs. All the while, you will receive the full traceability, documentation, serialization, and source inspection you require from our expert, onsite medical device manufacturing engineers. 

Brochure: Medical Device Manufacturing

Phillips-Medisize’s expertise in the medical device field provides a knowledgeable and trusted source for the successful development of concepts from drawing board to packaged product.
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