Nexcel® Medical Materials Validation to ISO 11607

Materials testing to increase your speed to market

The use of any packaging material as part of a Sterile Barrier System is controlled under the ISO standard 11607. In order to ensure complete compliance for its materials, Sealed Air started testing its new medical device packaging structures against this standard.
The testing of its first three materials was managed by independent consultants who specified test methods, third party suppliers and sample size. In addition all material testing and results analysis were overseen and submitted as a final report by the consultants.
The use of this data as part of a device manufacturers validation protocol can save over 6 months time and money and is a real innovation in customer commitment and care.
Contact us to learn more about how we can show you that Nexcel® materials comply with ISO 11607.

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