This three day course is the ideal external training opportunity for people needing to gain a basic understanding of computerised system validation. The knowledge gained will help attendees to validate systems within their own organisation for use in GxP (GLP, GCP, GMP, GDP and GPvP) environments, and to audit validated computerised systems to assure compliance with the applicable GxP regulations.
The course starts with an introduction to the regulatory requirements and the system lifecycle and then concentrates on the practicalities of validating computerised systems and auditing these systems.
The course provides a mixture of presentations, discussions and practical workshops.
This course will provide delegates with an understanding of the computerised system validation process, including:
Who should attend
Tutors will be comprised from the list below:
Nichola Stevens
Director and Principal Consultant, Nuncius Compliance (Course Principal)
Barry McManus
Consultancy Partner, Empowerment Quality Engineering Ltd
"I feel a lot more confident to validate computer systems including writing the validation plan, test scripts and validation report."
"The presentation was very good and the talk was very helpful to understand about CSV validation and supplier qualification."
"Clearly an expert on the topics and a great presenter. Happy to answer any questions and provide support."
19 Points
Please note this course will run in UK timezone.
Day 1 |
|
09:00 | Welcome, Introduction and Course Objectives |
09:45 | Why Validate? Regulations and Guidance on Computerised System Validation Overview of the regulations and guidance applicable to CSV and their key expectations |
10:30 | Break |
10:45 | The System Lifecyle The concept of the SLC and the key outputs from it |
12:00 | Lunch |
12:45 | The Validation Process The approach to validation for different system types and a look at some of the key deliverables |
14:00 | Project Introduction |
14:15 | Exercise 1 - User Requirements Capturing, agreeing and documenting the user requirements for a system |
15:15 | Break |
15:30 | Exercise 1 - feedback |
16:00 | Risk Management Risk management and its impact on validation. Identifying the deliverables required. Then group discussion on risk assessment for 3 systems |
17:00 | Questions and Answers Answers to any outstanding questions from Day 1 |
17:15 | Close of Day |
Day 2 |
|
09:00 | Supplier Assessment The different approaches to supplier assessment and the things to be considered when assessing a supplier |
10:15 | Exercise 2 - Supplier Assessment Planning a vendor audit with a focus on the key validation deliverables |
11:00 | Break |
11:15 | Exercise 2 - feedback |
11:45 | Test Overview and Test Planning The different test phases, the purpose of each test phase and things to be considered when planning and reporting testing |
12:45 | Lunch |
13:30 | Test Overview and Test Planning Continued |
14:15 | Test Script Design, Execution and Review What a good test script looks like and the key things to consider when creating, executing and reviewing a test script |
15:30 | Break |
15:45 | Exercise 3 - Creating a Test Script Create a test script based on user requirements created on Day 1 |
17:15 | Close of Day |
Day 3 |
|
09:00 | Exercise 3 feedback |
09:30 | Infrastructure Configuration and Qualification |
10:30 | Break |
10:45 | Validation Reporting Overview of the Validation Report and what should be included in it |
11:15 | Maintaining the Validated State The procedures and records needed to ensure the system remains fit for purpose |
12:30 | Lunch |
13:15 | Change Control Key concepts related to making changes to validated systems |
14:00 | Exercise 4 - Change Control |
14:45 | Exercise 4 - feedback |
15:15 | Break |
15:30 | Data Integrity and Security How can we assure the integrity and security of our data |
16:45 | Course Objective Summary and Panel Discussion |
17:00 | Close of course |
This course will be run completely online. You will receive an email with a link to our online system, which will house your licensed course materials and access to the remote event.
Please note this course will run in UK timezone.
You will need a stable internet connection, a microphone and a webcam.
Auditing Computerised Systems
Computerised System Validation
Management of the Training and Competency of Personnel in GxP and Research Environments
P01 Introduction to Computer Systems Validation
P04 Quality Assurance for Good Laboratory Practice
P08 The Auditing Course
P34 Practical Approach to Auditing Systems and Processes
RP04 Quality Assurance for Good Laboratory Practice REMOTE LEARNING
RP09 The Remote Auditing Course REMOTE LEARNING
RP34 Practical Approach to Auditing Systems and Processes REMOTE LEARNING
RP37 Auditing Computerised Systems REMOTE LEARNING
Webcast - Where Does Audit End?