Packaging Type

Match your medical device with the packaging format, materials and sterilisation process.

Validation Process

Package designs must be validated (qualified), and the packaging process must be validated and controlled.

Regulatory Overview

Review of relevant legislation and standards affecting sterile barrier systems in Europe.

Packaging Equipment

Determine the best packaging equipment to match your packaging design and process.

Sterilisation Compatibility

Choose the most suitable sterilisation process for the materials and packaging of your medical device product.

Find A Supplier

Select a suitable partner. Click here to see and contact the full list of SBA member companies.

    Membership is open to Manufacturers of Sterilisation products or related services, with sales in Europe. Affiliation is open to companies/trade associations/healthcare professionals who are Responsible Users of SBS or represent those that are. Potential members or affiliates also need to have implemented a quality management system certified by an accredited certification body.

    For more details see Why become a member?

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