Quality risk management for pharmaceuticals

Dr Tim Sandle shares his insight into quality risk management for pharmaceuticals, discussing the tools and techniques for risk management.



Quality risk management is a core requirement of the Annex 1 revision, with regulators nudging the industry towards adopting a proactive approach to risk assessment.

This webinar considers the appropriate areas to assess, including contamination control and sterility assurance.



Topic areas we cover include:


  • The fundamentals of risk management
  • The tools and techniques for risk management
  • The importance of a scientific and data driven approach to risk management
  • Gain insight through considering case studies in risk management
  • Learn how risk management can go wrong

Get free access to this on demand webinar

About the speaker:



Dr. Tim Sandle has over twenty-five years’ experience of microbiological research and biopharmaceutical processing. He is a member of several editorial 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.

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