With facilities in the United Sates, Europe, Mexico and Asia, Phillips-Medisize provides OEM customers the latest manufacturing and design technologies in each region around the world – shortening the supply chain while increasing cost competitiveness. The Phillips-Medisize global quality system also allows for a clear understanding of the regulatory environment and specific regional compliance standards.
Design and development centers located in the United States and Europe, complement regional manufacturing sites and deliver a complete package for project initiation through production and distribution. Phillips-Medisize's global capabilities include design, development, tooling, assembly, packaging, sterilization, testing, labeling, and label control. We also have expertise in analytical lab testing, including does volume, time to delivery, USP ID testing, and FTIR for medical devices and drug delivery systems. Furthermore, Phillips-Medisize can develop and integrate high-speed automation at any of our global sites.
The company's three-tier, global customer-centric engagement model allows Phillips-Medisize executives to have regular contact with customers' "C suite" occupants to assure strategic alignment. Phillips-Medisize Business Development Managers engage with customer department heads to drive new opportunities forward, while the company's plant based managers engage with customer operations personnel to assure supply chain continuity. This strategy – combined with sites located strategically around the world, capabilities from design to finished product, and managed under a world-class quality system – provides the highest level of customer satisfaction possible.
Powerful advantages on a global scale
As a global leader in design, engineering and manufacturing, Phillips-Medisize has a global footprint that provides molding, manufacturing, assembly, packaging and testing. We offer total solutions, strengthened through:
- Early involvement
- Engineering resources
- Project management
- Supply chain management
- Turnkey supplier
- Skilled workforce
- 24/7 operations
- Diverse market base
- State-of-the-art technology
Phillips-Medisize is committed to providing a full suite of capabilities worldwide, with the highest level of customer satisfaction.
Quality Assurance and Certifications
Phillips-Medisize meets or exceeds global medical device manufacturing requirements including Europe and Japan. Our quality certifications/registrations include:
- MHRA EU GMP compliance
- MHLW certification
- Certified to ISO 13485:2003
- Certified to ISO 9001:2008
- Medical device and drug delivery manufacturing facilities registered to FDA 21 CFR 820 and 21 CFR 210/211
Our environmental and product compliance standards include:
- RoHS-compliant manufacturing process
- UL CSA TUV certifications
- Certified to ISO 14001:2004
- Green policy