Key components to the ISO 11607 procedure. ISO 11607 is the principle guidance for validating terminally sterilized medical device packaging
admin 2018-05-10T07:13:28+00:00Stability Testing – Overview and Update admin 2018-05-10T07:13:28+00:00
Stability testing and monitoring in the drug development and manufacturing process. A critical step applicable to Food and Drug Administration (FDA) regulated products.