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Reducing risk through packaging, part 1: Understanding the nuances of ISO 11607
While ISO 11607 broke new ground in creating a common platform and language for validating sterile barrier packaging, medical device manufacturers still have numerous questions about how to comply with the standard.
Many of those questions have been answered in "Reducing risk through packaging, part 1," written by members of the Sterilization Packaging Manufacturers Council (SPMC)—including Geoff Pavey, Oliver-Tolas Principal Engineer, Packaging Development—and published in Pharmaceutical & Medical Packaging News. The article is a follow-up to the group's February 2008 webcast "Understanding the Nuances of ISO 11607." The SPMC members previously published "Complying with ISO 11607: What will TIR 22 do for you? (part one and part two)" in PMP News.
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