Course No 16761Computer Validation: Introduction to Risk Management
19 November 2019, Copenhagen, Denmark
Non-ECA Members: EUR 890,--
ECA Members: EUR 790,--
EU GMP Inspectorates: EUR 445,--
APIC Members (does not include ECA membership): EUR 840,--
(All prices excl. VAT)
Tel.: +49 (0)6221 / 84 44 0 E-Mail: firstname.lastname@example.org
If you have any questions, please contact us:
You can find all other dates of this seminar in this overview.
Frank Behnisch, CSL Behring GmbH
Yves Samson, Kereon
Dr Robert Stephenson, Rob Stephenson Consultancy
- You get to know the current risk management approaches of ICH Q9 and the GAMP®5
- You become familiar with the latest methods and tools for risk analysis and can assess their relevance to practice in the validation of computerised systems
- You learn how the activities involved in the validation of computerised systems can be controlled efficiently by means of risk management
- In 4 workshops you can apply the procedures and discuss them
The current GMP regulations and guidelines (ICH Q9, GAMP®5, draft EU GMP Guide Annex 11 „Computerised Systems“) focus more and more on the topic of risk management. However, the regulations do not offer much concrete advice on how its principles should be translated into practice during the validation and operation of computerised systems. Therefore, it is the aim of this course to provide you with practice-oriented guidance in performing this task.
This Education Course is directed at employees from Production, Quality Control / Quality Assurance, Engineering, IT who have to deal with risk assessment and risk management in the field of computer validation.
Introduction – What do you want from this day?
An Introduction to Risk Management (including ICH Q9)
- Capturing delegates expectations
- Sharing and reducing to key points in groups
- Sharing with all delegates and tutors
Risk Management the GAMP® 5 Way
- Definition of “Quality Risk Management”
- Principles of Quality Risk Management
- Application of the principles in validation
- Methods of assessing and controlling risk
- Regulatory expectations for risk management
An Introduction to Risk Ranking
- The GAMP methodology for risk management
- Where to apply risk management in validation
- Methods of assessing risk
Assessing and Selecting a Supplier
- What is risk ranking
- How is it carried out
- How is it documented?
- A few useful applications
Workshop 1: Risk Assessment in Validation
- What are the criteria to use to select a supplier?
- Why does supplier selection matter?
- How should the selection process be conducted?
In this workshop, delegates will use the GAMP methodology. The participants will work on a case study in which the risks associated with a computer system are assessed and managed to reduce the testing workload in validation.
- Risk management applied to a computer system
- Evaluating identified risks
- Classification of risks into H, M, L
- Controls to mitigate unacceptable risks
- Links to the validation plan and protocols
Workshop 2: Risk Management in Validation
Based on a real case study, delegates will use the same risk assessment techniques to determine where to focus the qualification of a packaging line
- Risk management applied to a control system
- What are the conclusions from the risk assessment?
- What options do you have to mitigate (reduce) the higher risks?
- How will the output affect the protocol?
Workshop 3: Applying Risk Ranking to determine periodic review priorities
Delegates will apply the techniques of risk ranking to determine which systems present the highest risk to the patient and should therefore be reviewed first.
- How is severity determined?
- How can scales be created?
- Ranking the risks
- Developing a risk-based action plan.
Workshop 4: Assessing and Selecting a supplier
Delegates will assess supplier selection information to choose between two possible suppliers for an application.
- What factors influence supplier assessment?
- What risks are associated with supplier selection?