Event Type: STERIS AST Webinar | Date: December 2, 2021 - December 2, 2021 | Location: Webinar

11:30 EST

STERIS AST has been accepted as a participant in the FDA’s Ethylene Oxide Master File Pilot Program.  Join us in the webinar for an introduction to the Pilot Program and learn about eligibility requirements for creating a streamlined and flexible regulatory process when converting to a Sustainable EO® sterilization cycle and/or adding processing redundancy.


Brian McEvoy, senior director, global technologies

Scott Beard, senior director, quality systems and regulatory compliance

Bill Brodbeck, senior director, regulatory affairs