Quality risk management for pharmaceuticals

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

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.