Computerised System Validation: Introduction to Risk Management - Online Training Recording

Computerised System Validation: Introduction to Risk Management - Online Training Recording

Costs

ECA-Member*: EUR 790,--
Regular Fee*: EUR 890,--
EU/GMP Inspectorates*: EUR 445,--
APIC Member Discount*: EUR 840,--

(All prices excl. VAT)

* also payable by credit card American Express Visa Mastercard

If you have any questions, please contact us:
Tel.: +49 (0)6221 / 84 44 0 E-Mail: info@concept-heidelberg.de

Speakers

Yves Samson, Kereon, Switzerland
Dr Robert Stephenson, Rob Stephenson Consultancy, UK

Objectives

  • Get to know the current risk management approaches of ICH Q9 and GAMP®5
  • Become familiar with the use of the latest methods and tools for risk analysis when validating computerised systems
  • Learn how the activities involved in the validation of computerised systems can be controlled efficiently by means of risk management
  • In 3 case studies you can see how these procedures are applicable

Background

Current GMP regulations and guidelines (EU-GMP Guide Annex 11 ‘Computerised Systems’, ICH Q9, GAMP®5, ASTM E2500-13) 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.

Target Group

This Online Training 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.

Technical Details

To participate in an on demand training course or webinar, you do not need any software. The recordings are made available via a streaming server. In general, the recording is provided in MP4 format, which any PC (Microsoft Windows, Apple IOS) or tablet can easily display.

Timing and Duration:

When you register for the on demand Training course or webinar you can decide at what date you want to follow the training course online. For a 1-day training course you will have 2 days in which the stream is available (for 2-day training course 3 days and for a 3-day training course 4 days). Within in this timeframe you can start & stop the stream according to your needs.

In time before the scheduled date (your desired date) you will receive an e-mail from us with a link for direct participation as well as your log-in data.

Training Course Documentation and Certificate:
 
The presentations will be made available as PDF files via download shortly before the online training course. After the event, you will automatically receive your certificate of participation.

Programme

Computerised System Validation: Introduction to Risk Management
 
Introduction – What Do You Want From This Day?
  • Capturing delegates expectations
  • Sharing and reducing to key points in groups
  • Sharing with all delegates and tutors
An Introduction to Risk Management (including ICH Q9)
  • 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
Risk Management the GAMP® 5 Way
  • The importance of Risk-based Decision Making
  • How the GAMP® 5 Risk Management Approach aligns with ICH Q9
  • The 5-Steps you will need to follow described in detail
  • Risk Management throughout the System Lifecycle
  • Short workshop on Risk Identification and Risk Analysis
Risk Assessment the GAMP® 5 Way
  • The simple GAMP® 5 Risk Assessment Method
  • Assessment Scales for computerised systems that work
  • Functional Risk Assessments and Risk Reduction Strategies
  • Using risk to determine Test Rigour
Case Study: Risk Management Applied to a Computerised System
  • Evaluating identified risks
  • Classification of risks into H, M, L
  • Controls to mitigate unacceptable risks
  • Links to the validation plan and protocols
Case Study: 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?
An Introduction to Risk Ranking
  • What is risk ranking
  • How is it carried out
  • How is it documented?
  • A few useful applications
Case Study: Applying Risk Ranking to Determine Periodic Review Priorities
  • How is severity determined?
  • How can scales be created?
  • Ranking the risks
  • Developing a risk-based action plan.
 
Recording from 16 November 2021
Duration of the recording: approx. 5 h 8 min

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