Quality and Compliance

ISO 13485:2016 is recognized by regulators around the world as a good basis for addressing medical device design and manufacturing regulatory requirements. It allows us to enhance product safety by proactively identifying and managing product and project risks. Becoming ISO 13485:2016 certified has allowed us to better control the consistency of manufactured products.

CPC manufactures a variety of Life Sciences and Chemical Management product lines in a cleanroom certified by an external testing service to meet or exceed ISO Class 7 at 0.5 micrometers per ISO 14644-1 (superseding the former Federal Standard 209E Class 10,000). Certification data can be provided upon request. Please contact us with any questions. View ISO Standards

CPC manufactures a variety of Life Sciences and Chemical Management product lines in a cleanroom certified by an external testing service to meet or exceed ISO Class 7 at 0.5 micrometers per ISO 14644-1 (superseding the former Federal Standard 209E Class 10,000). Certification data can be provided upon request. Please contact us with any questions. View ISO Standards

ISO 9001:2015 is a standard that ensures consistency of a product ordered by customers. Organizations with ISO 9001:2015 certification have demonstrated compliance to the ISO 9001:2015 requirements by an independent registration authority. CPC’s Quality Management System has been approved and certified under the ISO 9001:2015 standard.

CPC manufactures quick disconnect couplings and connections made from a variety of metal, plastic and elastomeric raw materials. The shelf life of a connector is dependent upon the connector materials and the storage conditions.

At CPC, a subsidiary of Dover Corporation ("Dover"), we are strongly opposed to the use of forced, bonded, involuntary, prison or indentured labor.