Location: Webinar

Our next webinar will be addressing how pharmaceutical manufacturing facilities can improve their material transfer bioburden control by utilizing our new STERIS VHP low-temperature surface biodecontamination process. With manual wiping operations and lack of continuous control and contamination risks when transferring goods from a lower grade classified area to a higher, this often creates bottlenecks in many facilities.

Our experts will focus on the operation, design, features, benefits and applications for the new STERIS VHP DC-A Atmospheric chambers to help with material transfer to aseptic manufacturing or a research facility. Guidance for process and equipment implementation, qualification, and process validation steps will also be shared during this webinar. 

Who Should Attend?

  • Aseptic Manufacturing Managers
  • Plant Designers
  • Validation Managers
  • Quality Managers
  • Plant Operations Managers
  • Process Engineers
  • Engineering Managers
  • Component Manufacturers 

Click Here to Register