Packaging for terminally sterilized medical devices - Part 3: Requirements for process development for forming, sealing and assembly
Abstract
This document specifies requirements for process development for forming, sealing and assembly of packaging for medical devices to be terminally sterilized, when utilizing heat sealing technologies. This document recommends minimum heat sealing equipment features to support subsequent validation, process control and monitoring. This document applies to both preformed sterile barrier systems and sterile barrier systems. This document utilizes the sterile barrier system specification to develop the process specification using the principles of risk management. This document is intended to be used prior to process validation. NOTE ISO 11607-2 provides requirements for process specification and process validation.
Begin
2024-11-28
WI
00102191
Planned document number
DIN EN ISO 11607-3
Project number
17600128
Responsible national committee
NA 176-03-07 AA - Sterile supply
