Location: Frankfurt, Germany
Join STERIS Life Sciences and industry peers for a two-day event on cleaning validation and process optimization. You will learn science-based strategies for overcoming common cleaning issues in pharmaceutical manufacturing.
We will also share how to streamline current processes and maximize production uptime at your facility as representatives from STERIS Life Sciences provide a comprehensive overview of upstream and downstream manufacturing – focusing on the biopharmaceutical and vaccine industries. We will also introduce techniques to improve cleaning performance and address key challenges, such as biofilm remediation, stainless-steel preservation and more.
STERIS Life Sciences has decades of experience supporting Customers in the pharmaceutical and biopharmaceutical industries. Our presenters have extensive knowledge of process cleaning validation, Good Manufacturing Practices, regulatory compliance and other key areas.
If you work in the pharmaceutical or biopharmaceutical industries, you do not want to miss this event.
Lunch and dinner will be provided on 13 June with a cocktail hour to follow. Lunch will be provided on 14 June. Breakfast is included with your hotel booking.
Cost: €95
Attendees will receive an invoice at the conclusion of the event.
Register for Cleaning Validation Seminar
Registration closes on 1 June.
Some presentations will be delivered in English.
Meet the Presenters
Paul Lopolito, Technical Services Senior Manager at STERIS, has over 25 years of industry experience. He provides global technical support for process cleaning, cleaning validation and contamination control, which includes field support, site audits, training presentations and educational seminars.
Paul holds a bachelor’s degree in biological sciences.
Cecilia Pierobon, Technical Service Manager at STERIS, has over four years of experience in the qualification of pharmaceutical equipment for production and laboratory environments, Good Manufacturing Practices (GMP) and regulatory compliance. She provides global technical support to STERIS Life Sciences Customers on cleaning validation, the development of cleaning cycles and cleaning chemistry applications.
Cecilia holds a master’s degree in engineering management.
Filip Quintiens, QA Validation Specialist at Sanofi, has over 20 years of experience in the biotechnology industry. He provides validation services for Sanofi Geel (Belgium), with a focus on optimization of qualification and validation methodologies. He also acts as quality assurance validation lead in major site projects.
Filip has excellent knowledge of Good Manufacturing Practices (GMP) and is a cleaning subject matter expert at the Sanofi Geel multi-product facility.
Filip holds two master’s degrees in engineering with a focus on bioengineering and chemistry.