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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 8 (100,000) and Class 7 (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.
- Class 7 (10,000) and Class 8 (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.