Event Type: Webinar | Date: Marzo 4, 2025 - Marzo 4, 2025 | Location:

Presented by Noel Gibbons, Technical Advisor-Packaging. 

Terminally sterilized medical devices, pharmaceuticals and other products that require a sterile barrier must be validated in accordance to ISO 11607. Sterile barrier testing ensures that the sterile packaging system effectively maintains sterility throughout the product’s shelf life and the sterile barrier prevents ingress of microorganisms or contaminants to the product, ensuring patient safety. This presentation will provide an overview of the tests that support the validation of sterile barrier systems and provide guidance on the standards typically used during operational qualification (OQ) and process/performance qualification (PQ) after transportation testing and shelf-life studies are performed.

The presentation will be followed by a live Q&A.

Tuesday 4th March, 08.30 GMT | 03:30 EST 

Tuesday 4th March, 16:30 GMT  | 11.30 EST