Location: Virtual | 10:00 a.m. – 11:00 a.m. ET*
It is vital to take a risk-based approach when dealing with patient safety. Join our complimentary webinar to explore the current landscape of Water for Injection (WFI) use in pharmaceutical products and discover why multiple-effect distillation remains a strong contender for enhanced risk management.
Learn how to assess threats in pharmaceutical product applications, select effective WFI systems to prioritize patient safety and balance sustainability. Explore the basics of moist heat sterilization and apply these insights to enhance your risk assessment and Contamination Control Strategy.
* 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 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.