Packaging Validation Training of Sterile and Non-Sterile Medical Devices According to ISO 11607 and ISO/DIS 23417

The training covers the following standards.

• ISO 11607-1 Packaging for terminally sterilized medical devices — Part 1: Requirements for materials, sterile barrier systems and packaging systems
• ISO 11607-2 Packaging for terminally sterilized medical devices — Part 2: Validation requirements for forming, sealing and assembly processes
• ISO/DIS 23417 General specifications and validation methods for non-sterile medical device packages in good distribution practice principles