Medical Packaging News

MET’s validation and qualification services are fully compliant with the latest version of:

EN ISO 11607-1:2006 Packaging for terminally sterilized medical devices.
Requirements for materials, sterile barrier systems and packaging systems.

A terminally sterilized medical device packaging system should allow sterilization, provide physical protection, maintain sterility up to the point of use and allow aseptic presentation and meet the Essential Requirements of the European Medical Device Directives.

Our laboratory service will test your sterile barrier system for strength and integrity, confirming your expiry date. We will also test the protective packaging in storage and transport to confirm performance of your complete packaging system.