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Match your medical device with the packaging format, materials and sterilisation process.
Package designs must be validated (qualified), and the packaging process must be validated and controlled.
Review of relevant legislation and standards affecting sterile barrier systems in Europe.
Determine the best packaging equipment to match your packaging design and process.
Choose the most suitable sterilisation process for the materials and packaging of your medical device product.
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. Potential members also need to have implemented a quality management system certified by an accredited certification body.
For more details see Why become a member?
Fill out the form below to enquire about becoming a member: