Location: Virtual | 10:00 a.m. – 11:00 a.m. ET*

Are you looking for a safer, more sustainable way to sterilize potential biohazardous waste? Join our complimentary webinar to learn how the VIRASURE Air Decontamination System, with its patented decontamination cycle for Finn-Aqua® BPS Sterilizers, enhances your sustainability efforts by eliminating plastic use, supports carbon-free energy use and boosts safety measures for facility environments, operators and service personnel.

Discover how this innovative system outperforms conventional heating decontamination sterilization methods. Utilizing an all-electric, coiled forced hot metal contact surface process, it is particularly effective for applications in pharmaceutical vaccine manufacturing and high-containment biosafety facilities.


* Please note that the webinar broadcast time is listed in the Eastern Time Zone (ET). If necessary, be sure to convert to your local time zone.



Meet the Presenter


Juha Mattila, Senior Manager of Technical Services

Juha Mattila | Senior Manager of Technical Services

Juha Mattila is Senior Manager, Technical Services on terminal sterilization applications, equipment, and process technologies for STERIS Life Sciences Moist Heat and VHP Sterilization and decontamination technologies, and WFI and Pure Steam Systems. He has Bachelor of Science with Honors in HVAC and Process Engineering, and Master of Engineering in Business Informatics. He has 25 years of experience within the pharmaceutical and medical device industries and related research, including R&D, engineering, and product management.

In addition to being an active member of the Parenteral Drug Association (PDA), the International Society for Pharmaceutical Engineering (ISPE) and the Finnish Biosafety Network, Juha has authored several technical articles and spoken at many industry events. He also contributes to the International Organization for Standardization (ISO), the European Committee for Standardization (CEN), Finland Standardization Organization (SFS) for national standards and supported the British Standards Institution (BSI) work groups considering these technologies.

Juha facilitated the STERIS Life Sciences Equipment and Service commentary provision through the PDA for the European Union (EU) Good Manufacturing Practices (GMP) Annex 1 draft, participated in the PDA EU GMP Annex 1 Workshop and presented along with the STERIS webinar series over meeting EU Annex 1 conformance on various GMP equipment technologies.