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Sub and Complete Assembly

Product Assembly, Sub Assembly, and Complete Assembly in Low to High Volumes

Your low- to high-volume product assemblies are in expert hands at Phillips-Medisize. Here, you benefit from the services of a world-class, cGMP-compliant supplier of manual, semi-automated, and fully automated assembly capabilities. 

On your behalf, we can assemble, test, and sterilize components or finished devices in Class 7 and Class 8 clean room environments. Phillips-Medisize is also FDA registered as a drug manufacturer/packager under 21CFR parts 210 and 211.

From managing the entire assembly, sub assembly or complete assembly process to performing full product testing, inspection, and packaging, Phillips-Medisize assembly capabilities result in cost-efficient, repeatable, precision components. 


Product Assembly, Sub Assembly and Complete Assembly Capabilities

  • Sub assembly and complete assembly
  • Class 7 and Class 8 clean room environments
  • FDA registered (21CFR parts 210 and 211), cGMP-compliant, lean facilities
  • 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



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