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Eurofins Biopharma Product Testing Switzerland >> List of Webinars and Seminars >> The Journey of Facility Validation in Switzerland: Overview of Quality Control requirements for Facility Qualification

The Journey of Facility Validation in Switzerland: Overview of Quality Control requirements for Facility Qualification

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Attendees will be given an overview of Facility Qualification consisting of the topics Environmental Monitoring (EM), and Utility Monitoring (UM), testing of gases, cleaning validation, contamination control strategy and deviations all under GMP compliance to ensure best output for your qualification activities. Guided by seasoned technical experts, the session will walk participants through different areas of facility qualification and share practical strategies for addressing common challenges in validation and routine testing.

Session Highlights:

  • Gain an overview in Environmental and Utility Testing, including Cleanroom qualification and the Qualification of clean water systems (WFI, PW, Clean Steam, Feed Water) to ensure GMP compliance and product safety.
  • Explore methodologies for Biological Indicators, gas testing, and implementing robust contamination control strategies.
  • Understand the role of the contamination control strategy and effective deviation management in continuous improvement.

About the webinar:

Registration fee: FREE

Language: ENGLISH

Our speakers:

Patrick Sadri, Technical Expert, Eurofins BioPharma Product Testing Switzerland 

Patrick Sadri is a seasoned microbiology and quality control expert with over a decade of hands-on experience in the pharmaceutical biotechnology sector with a strong focus on facility qualification projects and implementation of new laboratories. Holding a Master of Science (MSc) in Pharmaceutical Biotechnology, with a thesis in cell biology, Patrick has applied his deep scientific knowledge to advance microbiological standards and practices across clinical and commercial production environments. 

Jean-Baptiste Sauvet, PhD, Head of Customer Service Microbiology, Eurofins BioPharma Product Testing Switzerland 

Jean‑BaptisteSauvet is part of the Customer Service Microbiology team at Eurofins BioPharma Product Testing Switzerland. With a PhD in physico‑chemistry and more than 15years of experience in pharmaceutical microbiology, GMP operations, and nanotechnology, he has built and launched GMP‑compliant microbiology production, R&D and contract‑service laboratories, assembled dedicated teams, and established robust GxP frameworks together with comprehensive documentation. His work focuses on developing and delivering tools and methods for assessing pharmaceutical decontamination, optimizing aseptic production processes, and driving strong Annex1 compliance while advancing strategic market positioning.

Marcel Goverde, PhD, FvP/ Responsible Person (RP), Eurofins BioPharma Product Testing Switzerland 

After studies in biology at the University of Basel, Marcel led from 2002-2010 several QC labs for microbiological quality control at F. Hoffmann-La Roche Ltd, Switzerland. From 2010-2011 he worked as a QC expert for microbiology at Novartis Pharma Ltd, Switzerland. Since 2011 he has been running his own business for consulting and training in microbiological QC and hygiene. Marcel is a regular speaker at different institutions, has written several scientific papers and edited a book. Since 2003 he is the Swiss expert in the EDQM Group 1, Microbiological Methods and Statistical Analysis.

 

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For further information feel free to contact us!