In this webinar, you will learn:
Single-use technology (SUT) is well established in all stages of bioprocess manufacturing, including upstream, downstream, and fill/finish unit operations. The implementation of SUT usually starts with development of the user requirement specification (URS). The end users at biopharmaceutical companies work closely with the supplier to select components and assemblies (standard or custom) to meet the application requirements. Single-use qualification and regulatory considerations can include properties such as physical, functional, biological, chemical and sterilization.
This webinar will discuss best practices for single use qualification including quality and regulatory documentation.
An on-demand version of this webinar will be available after the live event using the same link. Register now and access the webinar at your convenience.