Packaging validation of medical devices – Impact of the ISO 11607 revisions and appropriate strategies
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The medical device industry is a rapidly changing environment that is constantly adapting to the ongoing challenges within the medical landscape. One such challenge is designing an evaluation plan to meet the requirements for an appropriate and validated packaging system using package testing that meets FDA or international health and safety regulations. This webinar will mainly focus on packaging systems for sterile products; However, there are several test models suitable for packaging non-sterile products.
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