Sterile Barrier Packaging Systems

Worst-Case Assessment for Performance Testing

The term sterile barrier system was introduced in ISO 11607-1:2006 to describe the minimum packaging required to perform the unique functions required of medical packaging for terminally sterilized medical devices.

Adequately defining and capturing a worst-case justification for testing families of products from package verification testing to aseptic presentation can be difficult. Network Partners’ team of packaging engineering professionals can analyze your packaging data, to provide a worst-case justification and test plan for evaluating a family of packaging configurations.