EN ISO 11607-3:2026

Packaging for terminally sterilized medical devices - Part 3: Requirements for process development for forming, sealing and assembly (ISO 11607-3:2026) EN ISO 11607-3:2026

Publication date:   Aug 29, 2026

General information

60.60   Standard published   Sep 30, 2026

CEN

CEN/TC 102 Sterilizers and associated equipment for processing of medical devices

European Norm

11.080.30   Sterilized packaging

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Scope

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.

Life cycle

NOW

PUBLISHED
EN ISO 11607-3:2026
60.60 Standard published
Sep 30, 2026




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