Harries J E
Isotron, Elgin Industrial Estate, Swindon, UK.
Med Device Technol. 1998 Jul-Aug;9(6):18-21.
Potential solutions to some of the practical problems experienced when validating products processed by radiation sterilization are discussed in this article. The standards for validation and routine control of radiation sterilization are to be revised next year and there is now an opportunity for the industry to influence the effectiveness of those revisions. Medical device manufacturers are encouraged to make views known to help ensure a simpler standard that is widely implemented.
本文讨论了在验证经辐射灭菌处理的产品时遇到的一些实际问题的潜在解决方案。辐射灭菌的验证和常规控制标准将于明年修订,目前行业有机会影响这些修订的有效性。鼓励医疗器械制造商发表意见,以帮助确保制定一个更简单且能广泛实施的标准。