Packaging Validation of Medical Devices - Impact of the Revisions of ISO 11607 & Suitable Strategies

The medical device industry is a fast changing environment that is continuously adapting to the constant challenges within the medical landscape. One such challenge is designing an evaluation plan for fulfilling the requirements for a suitable and validated packaging system using package testing that will comply with FDA or international health and safety regulations. This webinar will mainly focus on packaging systems for sterile products; however, several test models are suitable to be used for packaging of non-sterile products.