Amcor Flexibles serves the global medical device market with 14 manufacturing sites located in Belgium, Brazil, France, Ireland, Italy, Portugal, Singapore, Spain, the United Kingdom, and the United States, including Puerto Rico. All plant quality systems are ISO 9000 registered and in compliance with cGMPs. Our U.S. plants are ISO 13485 registered, the medical device quality standard. Amcor offers you an in-depth understanding of the industry’s regulatory, quality and cGMP requirements, including: validated processes and design control, full product traceability, specification compliance, documentation systems, and process capability analysis (Cpk).
Equipped with the broadest technology base in the industry, Amcor Flexibles customizes packaging solutions to individual requirements for package configuration, performance, processing, opening features, and sterilization.
Coating Technology
Lamination Technology
Extrusion Technology
Finishing Technology
Printing Technology