Location: Virtual | 10:00 a.m. – 10:30 a.m. ET
Whether your operation specializes in pharmaceutical manufacturing, biotechnology manufacturing, or laboratory research, your process likely involves steam sterilization.
STERIS’s Finn-Aqua® BPS Sterilizers are developed for component and terminal sterilization, with models that are optimized to facilitate the most demanding current Good Manufacturing Practices (GMP) for pharmaceutical and biotechnology manufacturing. Non-GMP research applications are also supported.
During this webinar, we review how our new, consolidated Finn-Aqua BPS Sterilizer platform provides GMP and research capabilities to meet your needs.
Topics include:
- An overview of the new Finn-Aqua BPS Sterilizer platform for GMP and non-GMP operations
- STERIS’s comprehensive GMP documentation for installation, operation and performance qualification
- The new Self-Cleaning Drain Strainer option
- How STERIS can support your steam sterilization requirements
* 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.
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Meet the Presenter
Jaakko Kurikka is a Product Manager of Sterilization Technologies at STERIS Life Sciences. He has over a decade of experience in steam sterilization, manufacturing and sourcing processes. He holds a bachelor’s degree in business and technology.
With an in-depth knowledge of all STERIS Finn-Aqua equipment offerings, Jaakko has spent most of his time with the company on the purchasing team as a Senior Sourcing Specialist. He supports operations and research and development for all STERIS Finn-Aqua operations and research and development.
Jaakko is an active member of the Finnish Standards Association. He serves as a member of multiple sterilization technical committees for the organization, including CEN/TC 102 - Sterilizers for Medical Purposes, CEN/TC 204 Sterilization of Medical Devices and ISO/TC 198 - Sterilization of Healthcare Products.