This webinar will touch on some of the changes implemented with the release of the MDR’s in the European Union and the impact to the packaging requirements. Specifically these new regulations prompted the changes to the packaging industry resulting in the newly published ISO 11607. A discussion on 3 key points regarding packaging will be discussed and how the ISO 11607 directs device manufacturers to meet these changes. Additionally a brief discussion on the life cycle approach to packaging validations including an in-depth look at a couple specific tests and finally a high level look at sample size considerations as part of the establishing a validation testing plan.
