PDA Universe of Pre-Filled Syringes and Injection Devices Conference 2025
Visit us to learn how you can sterilize your temperature- or radiation-sensitive drug products.
Austria Center Vienna · Vienna, Austria
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Join us at the PDA Universe of Pre-Filled Syringes and Injection Devices Conference, booth #73, to learn how you can sterilize your temperature- or radiation-sensitive drug products with the VHP LTS-V Low Temperature Sterilizer—designed specifically for in-house sterilization.
At the show, don’t miss our technical talk and poster presentation—see full details below.
Presented by: Juha Mattila – Senior Manager, Technical Services
21 October 2025 | 10:50 – 11:00
Explore the application of VHP sterilization for RTU containers, with emphasis on regulatory requirements, process validation and material compatibility.
Presented by: Juha Mattila – Senior Manager, Technical Services
Learn how the FDA’s recognition of VHP as an established sterilization method supports safer, more flexible options for medical and combination devices, especially those sensitive to heat or radiation.
Juha has over two decades of experience in pharmaceutical, medical device, research and biosafety technologies, with expertise in moist heat and Vaporized Hydrogen Peroxide (VHP™) sterilization, VHP biodecontamination technologies and Water-for-Injection (WFI) distillation and pure steam 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.
At STERIS Life Sciences, Juha serves as a Senior Manager of Technical Services for sterilization applications, equipment and critical utilities technologies. He provides technical leadership across sterilization and biodecontamination systems and supports global Customers with complex equipment and utility related needs.
Juha is an active member of the Parenteral Drug Association (PDA), a Nordic Board member for the International Society for Pharmaceutical Engineering (ISPE) and a member of the Finnish Biosafety Network. He has authored several technical articles and presented at numerous industry events. He also contributes to standards development through involvement with the International Organization for Standardization (ISO), the European Committee for Standardization (CEN), the Finnish Standardization Organization (SFS), ASTM International and the British Standards Institution (BSI). Juha also coordinated the STERIS Life Sciences Equipment and Services 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 Workshops in 2022 and 2024.
Your needs are unique – so is our approach. Discover how a partnership with STERIS can reduce risk and improve sustainability and efficiency at your facility.
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