Single use systems (SUS), sometimes referred to as bioprocessing systems, have increased in popularity due to their advantages over the stainless-steel pipes and tanks. Along with these advantages there are also complications in the form of determining an appropriate radiation sterilization dose (for the manufacturer) and appropriately “verifying” sterility (for the manufacturer or the end user).

In addressing both of these issues, occasionally approaches are taken that are either incorrect from a scientific perspective or that are unnecessarily arduous. This webinar will explore options to simplify and to correctly address both issues.

In this webinar you’ll learn:

• Options already present in the standards that can simplify determination of a radiation sterilization dose 
• Appropriate ways to “verify” sterility for single use system subassemblies or finished products
• Available and upcoming resources for sterilization validation and sterile verification of single use systems 

• Sterility assurance personnel
• Validation personnel
• Sterilization microbiologists
• Quality assurance personnel
• Product engineers