Nolan P J
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Webinars on the revisions to ISO 11607, Packaging for Terminally Sterilised Medical Devices, have prompted many questions from manufacturers and package engineers concerned with validating their packaging under the new requirements. A selection of those questions are reviewed here.
关于《最终灭菌医疗器械包装》ISO 11607修订版的网络研讨会引发了众多制造商和包装工程师的诸多问题,他们关注如何根据新要求对其包装进行验证。以下对其中一些问题进行了回顾。