Medical Packaging News

Validation of package seal strength and integrity is required for CE marking and FDA submissions for medical devices. Testing is also required following realistic transit simulation and shelf life aging.

MET’s comprehensive service ensures that you document your compliance to parts 1 and 2 of ISO 11607 (Packaging for terminally sterilized medical devices.

Part 1:
Requirements for materials, sterile barrier systems and packaging systems,

Part 2:
Validation requirements for forming, sealing and assembly processes).

Our internal laboratory provides sterile barrier and packaging system testing for your packaging. Our engineers provide on site validation of your packaging equipment. Download our ‘How To Guide’ here.

Medical Device Packaging Test