Clean Room Packaging

With patient safety dependant in part on the integrity of our packaging, Barger ensures strict adherence to its ISO 9001:2008 and ISO 13485:2003 certifications while also supporting international quality standards and guidelines including ISO 11607-2 and 21 CFR 820.

Packaging experience that matters

From low to high volume runs, whether developing packaging for orthopaedic implants or cardiac stents, Barger creates innovative medical device packaging systems in our GMP-oriented, lean manufacturing clean room facilities helping ensure package cleanliness from production to final end use. Our experienced engineering, quality and account managers work hand-in-hand with your engineering team to meet tight production specifications and timelines.

Controlled environements

With growing regulatory requirements, sterile pharmaceutical and medical device packaging is produced and packaged in our meticulously controlled ISO certified Class 8 clean room facilities. Our experienced and knowledgeable operations and QA team ensure strict quality control procedures are upheld throughout the entire packaging process from prototyping, thermoforming, welding, die-cutting, printing and packaging. Our protective BargerGard® and pre-validated BargerVPAK™ products are also formed and welded in our clean room environments ensuring production within a controlled environment minimizing contamination.

At Barger we help create medical packaging success stories. With innovative engineering, creative manufacturing and a collaborative environment, it’s a winning combination that puts your needs at the center.

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