We use cookies to give you the best experience and to help improve our website
We use cookies to make our website easier to use and to better understand your needs.
Jump to content
Standards Development is a service provided by BSI Group
Packaging for terminally sterilized medical devices. Requirements for materials, sterile barrier systems and packaging systems
Packaging for terminally sterilized medical devices. Validation requirements for forming, sealing and assembly processes
Packaging for terminally sterilized medical devices. Guidance on the application of ISO 11607-1 and ISO 11607-2
Safety requirements for electrical equipment for measurement, control and laboratory use. Particular requirements for cabinet X-ray systems
Packaging for terminally-sterilized medical devices. Method for determination of methylene blue particulate penetration
Safety requirements for electrical equipment for measurement, control and laboratory use. Particular requirements for automatic and semi-automatic laboratory equipment for analysis and other purposes
Sterile packaged ready for filling glass cartridges
Sterile packaged ready for filling glass vials