Factory Acceptance Testing for Parts Washers: Confirming Performance Before Installation
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Factory Acceptance Testing (FAT) provides the opportunity to test and verify the proper operation and performance of washing equipment before installation in your facility. Join our complimentary webinar to learn why FAT is a critical step in confirming your equipment’s effectiveness, ensuring confidence and compliance across validated cleaning processes.
Gain a comprehensive understanding of FAT, including what to expect during a facility visit, from pre- and post-delivery documentation to component performance evaluation, coverage testing, configuration checks and accessory and rack verification. Explore key industry guidelines and understand the relationship between FAT and process validation.
Olivier has over a decade of industry experience, with expertise in product portfolio management for Good Manufacturing Practices (GMP) and research washer and steam sterilization technologies.
He holds a bachelor’s degree in business marketing.
At STERIS Life Sciences, Olivier is responsible for developing long-term vision and strategy for several product lines, as well as the tactics required to implement that vision. He also oversees new product and market development, monitors evolving industry standards and regulations and provides product training to support company objectives.
Olivier is an active member of the International Society for Pharmaceutical Engineering (ISPE) and the Parenteral Drug Association (PDA). He has coauthored several articles featured in scientific publications and has spoken at industry events for ISPE, PDA and other associations.
Paul has over two decades of industry experience in pharmaceutical manufacturing and laboratory research settings, with expertise in process cleaning, cleaning validation and contamination control.
He holds a bachelor’s degree in biological sciences.
At STERIS Life Sciences, Paul provides global technical support through field consultations, site audits, training presentations and educational seminars. He also manages the Process and Cleaner Evaluation (PACE™) program and analytical testing laboratory, which simulate Customer cleaning processes and support analytical method development and validation.
Paul is experienced in managing cross functional projects related to process cleaning and critical environment operations, with direct experience in the biopharmaceutical and biomedical device industries. He is a frequent speaker at industry events and has published several articles and book chapters related to cleaning validation and contamination control. He is also an active member of the International Society for Pharmaceutical Engineering (ISPE) and the Parenteral Drug Association (PDA).
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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