Location: Virtual | 10:00 a.m. – 11:00 a.m. ET*
Recent regulatory developments impact several process standards that your facility must meet to achieve compliance. Join our complimentary webinar where we explore recent regulatory developments affecting moist heat sterilization processes and sterilizer equipment in pharmaceutical manufacturing.
Learn about the implications of updated regulatory guidelines and standards, such as EU Annex 1 and the revised moist heat sterilization process standard (ISO 17665:2024). Discover potential future developments, including ongoing work on liquid load sterilizer equipment (ISO 19253).
* 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 Matilla | Senior Manager of Technical Services
Juha has over two decades of experience in pharmaceutical, research and biosafety technologies. He manages the STERIS Life Sciences portfolio of products for Vaporized Hydrogen Peroxide (VHP) and steam sterilization, material transfer biodecontamination technologies and water for injection and pure steam generation systems. He holds a master’s degree in business informatics and a bachelor’s degree in heating, ventilation and air conditioning (HVAC) and process engineering.
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) and the British Standards Institution (BSI) work groups considering these technologies.
Juha provided commentary through the PDA for the European Union (EU) Good Manufacturing Practices (GMP) Annex 1 draft and participated in the PDA EU GMP Annex 1 Workshop.