Understanding and Implementating Quality Risk Management

  • Product Id : FDB2302
  • Category : , ,
  • Presenter :
  • Scheduled On : December 17 2019 1:00 pm
  • Duration : 60 Minutes

Attendees will come away with the ability to recognize the purpose and value of Quality Risk Management QRM, explain the level of risk based on severity, occurrence, and detectability and how the QRM process is used to make decisions. In addition they will be able to identify key QRM terminology and recognize the four (4) key components of Quality Risk Management. Finally they will have a strong understanding of the key concepts associated with the risk management risk tools and their application.

Why You Should Attend:

Per ICH Q10 Quality risk management is integral to an effective pharmaceutical quality system. It can provide a proactive approach to identifying, scientifically evaluating and Controlling potential risks to quality. However integrating the principles of QRM into our quality processes is complex especially in a pharmaceutical organization. There is much confusion on how to define risk and individuals often think of quality risk management as just a tool like FMEA analysis verses an overall QRM approach. This training will explain the important concepts associated with a QRM approach.

Areas Covered in the Session :

  • Recognize the purpose and value of Quality Risk Management (QRM), as well as how it applies to your job
  • Explain the level of risk based on severity, occurrence, and detectability and how the QRM process is used to make decisions
  • Identify key QRM terminology
  • Recognize the four (4) key components of Quality Risk Management
  • Identify examples of QRM tools and their application
Who Should Attend:

  • Quality Departments
  • Regulatory Departments
  • Compliance Departments
  • Production Departments
  • Manufacturing Departments
  • Engineering Departments
  • Process Owners
  • Development
  • Auditors


Steven Laurenz

Steven Laurenz, Principal Consultant – BioPhia Consulting Inc., has over 25 years of technical leadership experience in product development, process development, technology transfer, and process optimization. He is skilled in taking new products from early laboratory stage to successful manufacturing launch. He is an expert in integrating Quality by Design and risk management into product development. He has proven experience in establishing a Quality System for a R&D Quality Assurance organization.

Steven has headed product development departments at Abbott Laboratories and AbbVie Inc. and held leadership positions in numerous technical consortium.

Steven Laurenz holds an M.S. in Chemical Engineering from the Michigan State University



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  • Presentation Handout in .pdf format
  • Presentation from the Speaker
  • Feedback form
  • Certificate of Attendance
  • Recording access Information with Password to view the webinar, will be sent 24 hours after the completion of the Live webinar.
  • Presentation Handout in .pdf format
  • Certificate of Attendance