If there’s one constant in healthcare packaging, it’s change. We can help you navigate an ever-changing, often-challenging and increasingly complex healthcare and regulatory environment. In addition to providing a great portfolio of packaging technologies, we offer the expertise to deliver solutions with both value and innovation.
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Design & Testing
Whether in our lab or in your facility, our healthcare packaging engineers design solutions that reduce cost, improve material performance, increase productivity, and troubleshoot packaging failures.
With years of experience in the global manufacturing industry, we understand many of the global regulations you face. Let Oliver help you navigate them.
US-based manufacturers and distributors count on the expertise of our on site process validation services to guide you through the regulatory requirements established by the Food and Drug Administration (FDA) for Class I, II and III medical devices.
In 2020, new European Medical Device Regulation (EU MDR) will seek to increase medical device safety and effectiveness in the European market. We’re armed with the tools to help our customers meet the packaging challenges presented by these new protocols.
With an increase of on-site audits, our knowledgeable and experienced validation team can help ensure that our customers’ devices comply with regulations set forth by the China Food and Drug Administration (CFDA).
Technical Labs
Manufacturing Facilities
Employees
5
Technical Labs
7
Manufacturing Facilities
850
Employees
Our singular focus on healthcare packaging, combined with our global reach and local in-language support, enables us to deliver superior solutions, unsurpassed quality, and value to our customers.
