About the Webinar
Robust cleaning procedure is an important factor that can contribute to the success of the overall pharmaceutical manufacturing process. Common cleaning issues such as Air-Liquid Interface (ALI) rings, rouge, biofilm, and other challenging soils can increase the risk of product contamination, and adulterated drug product can affect patient safety. This presentation will enable the participants to understand the current regulations related to cleaning, and various factors that can affect the effectiveness of the cleaning process such as cleaning procedures. Examples of the cleaning challenges and its remediation procedure will be discussed in detail, together with case studies.
Paul Lopolito is a Senior Technical Services manager for the Life Sciences Division of STERIS Corporation.Paul is a frequent speaker at industry events including ISPE, PDA, INTERPHEX, ACS, ACHEMA, AALAS, LAMA, A3P, and IVT. Paul has published several articles and book-chapters related to cleaning validation and contamination control.
Richard Chai is a Technical Service manager in the Life Sciences Division of STERIS Corporation. Richard has more than 20 years of industry experience in manufacturing, validation and technical support. He has published several articles in contamination control and is a frequent speaker at industry events.
2 фев 2022
