Location:

Presented by: Juha Mattila | Senior Product Manager


Heat and radiation sensitive drug products in pre-filled syringes, or sterility-requiring implants and other devices can be challenging from a terminal sterilization perspective. In many applications, they may be required to be assembled and packaged individually in grade A or B areas since such applicable methods may not have been available for larger scale manufacturing processes.


Understanding the VHP (Vaporized Hydrogen Peroxide) deep vacuum sterilization process can help improve your critical manufacturing processes, improve product package sterility, cut operating costs, save time and improve product quality control.


In this webinar, Juha will explain the basic process principles of VHP low temperature surfaces sterilization in pharmaceutical manufacturing environments.  He will also explain the preferred approach for product feasibility testing and cycle development to benefit validation of production cycle.


Visit us at: STERISLifeSciences.com

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