Medical DeviceQualified Supplier Directory
Phillips-Medisize Company Profile
Qualifications: ISO 13485, ISO 9001, FDA Registered, CGMP Certified, Supplier to Medical Manufacturers, Exhibitor in at least 2 MD&M and/or MEDTEC shows
Markets Supplied: North America, Europe, Worldwide
Phillips-Medisize is a leading global outsource provider of design, development and manufacturing services to the medical device, diagnostics and drug delivery markets. For over four decades, Phillips-Medisize has been an innovator in the medical outsource design, development and manufacturing business. The company also has a complimentary commercial business. Phillips-Medisize provides its customers with the highest level of satisfaction, providing state-of-the-art technologies, innovative design and highly creative people with the skills to execute at a very high level on sophisticated projects.
With six design development centers in Wisconsin, California The Netherlands, Denmark, United Kingdom and China, Phillips-Medisize has over 500 full-time design and development professionals to provide comprehensive services for the world’s top medical OEMs. These OEMs rely on Phillips-Medisize’s unique, integrated phased design and development process for products such as drug delivery devices, diagnostic equipment and consumables, single-use surgical devices and primary pharmaceutical packaging. By partnering with Phillips-Medisize early in the design and development process, customers can realize enhanced speed to market, cost savings, risk mitigation and ultimately smooth commercialization of their products.
Phillips-Medisize has a robust quality management system process used at its plants around the world. The company’s QMS process is adaptable to global requirements, integrated for managing drug handling, and also supports class I, II, and III devices. This quality system provides a state of the art supplier management capability that is used in the outsourced manufacturing and design of finished goods, as well as, component products the company also manufactures. Our global facilities adhere to the most rigorous quality standards:
- FDA-registered sites compliant to 21 CFR 4, 210/211 and 820
- Certified to ISO 13485, 9001 and 14001
- MHRA EU GMP compliant
- MHLW accreditation certification
- RoHS-compliant manufacturing processes
Phillips-Medisize state-of-the-art facilities provide superior solutions in a full range of technologies ranging from plastic, silicone and metal injection molding. The company also provides complete solutions for packaging in the pharmaceutical, medical device, and drug delivery markets. Phillips-Medisize’s clean rooms feature manual, semi-automated, and fully automated production lines capable of handling millions of components or finished devices. Production lines are carefully designed and built to fulfill the special and individual needs of every customer and program.
To enhance customer value, Phillips-Medisize has developed an aggressive supply chain model, from technical sourcing and supplier quality engineering to production and logistics. With increased competition and globalization, Phillips-Medisize has driven a solutions-based supply chain process to support our customer’s requirements. This process consists of an active relationship management with customers and suppliers alike to keep all parties on the same wavelength.
Ultimately Phillips-Medisize’s goal is to partner with its customers to provide outsource design, development and manufacturing services which can accelerate speed to market and then work with these same customers to deploy advanced automated assembly and quality control technologies which, reduce manufacturing cost while improving quality.
For more information contact Phillips-Medisize