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Phillips Plastics is a world class supplier of manual, semi automated, and fully automated assembly capabilities. The Company has the ability to assemble, test, and sterilize components or finished devices in class 100,000 and 10,000 clean room environments. Phillips is registered by the FDA as a drug manufacturer/packager under 21CFR parts 210 and 211.
From managing the entire assembly process to full product testing, inspection, and packaging, Phillips Plastics assembly capabilities result in cost-efficient, repeatable, precision components.
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- Class 10,000 and 100,000 clean room environments
- FDA registered facilities
- Facilities are cGMP compliant
- In-house automation design and manufacture per GAMP
- Design and development services
- Low and high volume capabilities
- Protocol development and validation as well as computer software validation (CSV)
- Supply chain management including engineering development
- Full range of value-added secondary services
- Drug packaging
- Product packaging and analytical testing
- Facilities operate under lean principles
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Click here for a sneak peek into the Insulet OmniPod program, and see how one of the critical components, the chassis, uses MID technology to provide mechanical support and electrically isolated traces.