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A webinar as part of the Reading Scientific Services Ltd. series surrounding sterile pharmaceutical preparations

The webinars in this series are designed to cover critical steps, focusing on the requirements of Good Manufacturing Practice (GMP) and the essential elements needed to develop a robust sterility assurance system and contamination control strategy.

Learning outcomes

  • Understand the immediate actions to be taken in the event of a sterility test failure
  • Review the focal points for the laboratory failure investigations, from reviewing training to isolator controls
  • Find out how to construct a road map for process failure investigations, from filter controls to personnel interventions
  • Learn how to reach an outcome and to set effective follow-up corrective and preventative actions


Dr Tim Sandle has over twenty-five years' experience of microbiological research and biopharmaceutical processing. He is a member of several editorials boards and he has written over six-hundred book chapters, peer reviewed papers and technical articles relating to microbiology. Dr Sandle works for a pharmaceutical manufacturer in the UK, and is a visiting tutor at both the University of Manchester and UCL.


To register for this webinar, please visit the RSSL website.

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