Packaging standards continue to develop and evolve a decade after the most recent version of ISO 11607:2006 Packaging for Terminally Sterilized Medical Devices.  This presentation will provide an overview of the changes that are currently being discussed as well as working items that are under consideration that could affect the standards tomorrow. It will touch on the changes to the pharmaceutical packaging industry with regards to USP Guidance chapter <1207> PACKAGE INTEGRITY EVALUATION—STERILE PRODUCTS and Medical Device ASTM method work item developments and updates.