We are recognised around the world as the premier supplier of sterilisable medical device packaging.
Our expertise and product line breadth will provide you with the most cost-effective packaging solution to protect and maintain the sterility of your device until the moment the package is opened.
From packaging design through to validation, we offer a range of value-added services to supplement your in-house resources and reduce the time to market.
Our global manufacturing footprint
We serve the global medical device market from 15 manufacturing sites located in:
- United Kingdom,
- United States, including Puerto Rico.
All plant quality systems are ISO 9000 registered and in compliance with cGMPs. Our U.S. plants are accredited to the ISO 13485 medical device quality management standard.
We offer 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).
Knowledge & expertise
Equipped with the broadest technology base in the industry, we customise packaging solutions to individual requirements for package configuration, performance, processing, opening features, and sterilisation.