Location: Virtual | 10:00 a.m. – 11:00 a.m. ET*
Applied analytical methods enable precise evaluation of product contact surfaces, supporting the cleaning validation lifecycle through accurate residue detection and risk assessment. Join our complimentary webinar to explore various analytical methods including conductivity and Total Organic Carbon (TOC) Monitoring, Ultraviolet (UV) spectroscopy, Fourier Transform Infrared (FTIR) spectroscopy and Raman spectroscopy that confirm surface cleanliness.
Discover how one or more analytical methods can integrate into the cleaning validation lifecycle, their specific use cases and practical applications. Learn the advantages of UV in-line versus off-line spectroscopy for STERIS formulated detergents and understand how this approach helps operations save time, resources and provide real-time monitoring of cleaning processes.
* 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 Presenters
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Paul Lopolito | Director, Technical Services
With over two decades of industry experience in pharmaceutical manufacturing and laboratory research settings, Paul provides global technical support for process cleaning, cleaning validation, and contamination control, which includes field support, site audits, training presentations and educational seminars. He holds a bachelor’s degree in biological sciences.
Prior to joining STERIS Life Sciences, Paul spent three years as a Manufacturing Technical Services Manager at Massachusetts Biological Laboratories providing technical support and project management for the vaccine, monoclonal antibody, blood product and filling/packaging groups. He also spent time at TEI Biosciences, where he held positions of Research Associate, Laboratory Manager and Manufacturing Manager.
Paul manages the Process and Cleaner Evaluation, (PACE™) program for STERIS Life Sciences, which simulates a Customer’s cleaning process to make recommendations for improvements. He has expertise in managing cross-functional projects related to process cleaning and critical environment operation with direct experience in the biopharmaceutical and biomedical device industries.
Brian Bosso | Manager, Technical Services
Brian has over a decade of experience in developing and implementing cleaning validation process lifecycles, process design, analytical method development and validation, risk assessments and regulatory remediation. He holds a bachelor’s degree in chemistry.
Prior to joining STERIS Life Sciences, Brian held supervisory and management positions for multiple pharmaceutical and biopharmaceutical companies.
At STERIS Life Sciences, Brian provides global technical support for pharmaceutical detergents and other critical environment products and applications.
Brian is an active member of the Parenteral Drug Association (PDA) and the International Society for Pharmaceutical Engineering (ISPE).