Presented by
Management Forum
Understanding Computer System Validation (CSV) Training Course
A comprehensive and practical introduction
This course covers the key concepts of computer systems validation and provides practical guidance on how to comply with the regulations applicable to the pharmaceutical industry. It will include the regulatory requirements, the industry standards and best industry practice based on Good Automated Machine Practice (GAMP®5). It will provide a practical and efficient framework for computerised systems validation and compliance, and gives attendees an appreciation of how these ideas may be applied to their own systems and processes.
★★★★★ "My overall opinion is that this course was very worthwhile and well taught. I feel as though I learn... more"
24-25 July 2024
+ 25-26 November 2024 »
from £1099
- Format: Live online
- CPD: 12 hours for your records
- Certificate of completion
Overview
Computer Systems Validation (CSV) is a process used to test, validate and formally document that a regulated computer-based system does exactly what it is designed to do in a consistent and accurate manner that is secure, reliable and traceable. The system has to be relied upon to:
- produce data accurately and consistently
- create an indelible electronic data trail that is transparent, traceable and tamper-proof
- store electronic data records in a way that is safe, secure and can stand the test of time
Computerised system validation and compliance is a regulatory requirement. Inadequate or inappropriate validation can lead to serious non-compliance and quality problems. Compliant and validated computer systems are a prerequisite for effective data integrity.
This course covers the key concepts of computer systems validation and provides practical guidance on how to comply with the regulations applicable to the pharmaceutical industry. It will include the regulatory requirements, the industry standards and best industry practice based on Good Automated Machine Practice (GAMP®5).
This course will provide a practical and efficient framework for computerised systems validation and compliance, and gives attendees an appreciation of how these ideas may be applied to their own systems and processes.
This course is part of our GxP training (Good x Practice) course collection, which features a variety of topic areas to ensure you comply with the most recent quality guidelines. For more information on the latest EU GMP regulations, see our GMP training course covering the Annex 1.
Benefits of attending
- Gain a comprehensive overview of computer system validation (CSV)
- Enhance your understanding of the key terms used in CSV
- Recognise how Good Practices apply to computerised systems
- Understand the different approaches which might be employed
- Learn how to manage the risk associated with data integrity
Who should attend
- Quality management specialists
- Pharmaceutical validation professionals
- Pharmaceutical project managers
- Computer system engineering specialists
The Understanding Computer System Validation (CSV) course will cover:
Terminology
- Key terms
- Common acronyms
Overview of computer system validation (CSV)
- Introduction to CSV
- Why is it so important?
- Regulatory requirements
- FDA’s 21 CFR Part 11
- Other regulatory guidelines
- International regulations (EudraLex Volume 4 — Annex 11,ICH, WHO)
- The GAMP framework
Where to start
- How to manage electronic data
- Risk-based approach to CSV
- Audit readiness
- Exercise: data integrity
Types of computer system
- Business system
- Standalone control systems
- Equipment control systems
- Infrastructure
The six elements
- Hardware
- Infrastructure
- Software
- Data
- Documentation
- Records
- Exercise: creating an infrastructure map
Validation documentation
- Inventory
- SOPs and protocols….
- Records
- Training
- Change control
Industry standards
- cGMP
- GAMP®5
- Validation
- Eudralex
- CFR
- PIC/s
- Exercise: risk management
Q & A
Introduction and recap of Day 1
Practical application
- A risk-based approach
- The V model
- Software
- Hardware
- Exercise: putting them together
Validation in phases
- Concept
- Project
- Operation
- Retirement
- Exercise: Supplier involvement
Validation planning
- Risk-based decisions
- Supplier assessment
- Activities
- Deliverables
- Responsibilities
- Exercise scaling effort
Protocols and testing
- Test relationships
- Structure
- Requirements
- Managing change
- Exercise: summary report
System validation
- Software validation
- Installation Qualification
- Operational Qualification
- Performance Qualification
- Exercise: what comprises validation
Data migration
- Upgrades
- New systems
- Planning and testing
- Automation vs Manual
- Exercise: the process
Wrap up and Q & A
Paul Palmer
Paul R Palmer Ltd
Paul R Palmer is a Director / Pharmaceutical Consultant and a practicing EU / UK Qualified Person. He has over 35 years experience in the pharmaceutical industry in the development, manufacture and supply of medicinal products and medical devices.
Throughout his career, Paul has intentionally taken on all opportunities as they arose in order to develop a broad range of knowledge with an in-depth detailed understanding of manufacturing, storage, distribution, research, computerised systems, as well as the facilities and services to support each.
People and systems have always been a core focus, how to ensure best use, optimise and enhance efficiency. He has a level of curiosity rarely displayed in people taking on the qualified person role in pharmaceutical manufacturing. Culture, behaviour and psychology are all significant influences on the systems and processes we implement, but are often ignored.
Paul studied psychology as part of his MSc in 1993 and has always enjoyed observing the world around him with a curiosity that is rarely satisfied.
Farah Nadeem
Paul R. Palmer Limited
Farah Nadeem is an Operations Manager at Paul R. Palmer Limited/ Pharmaceutical Consultant and a Trainee Qualified Person. Farah is a Pharmacist and recognised QA expert and has over 20 years of experience in the Pharmaceutical industry in the development, manufacture and supply of medicinal products.
Throughout her career, she has held various quality assurance roles and actively pursued new opportunities to expand her knowledge and expertise. As a result, she has gained a comprehensive understanding of manufacturing, storage, and distribution processes, as well as the facilities and services that support them. Involved in documentation management: writes, reviews, and audits SOPs and QMS implementations. Assists companies in meeting regulatory requirements.
In her current role as a QA Operations Manager for a Pharmaceutical Consultant Company, Farah Nadeem provides various solutions, including assistance in obtaining the first MIA(IMP) and MIA licenses, as well as preparation and hosting for regulatory inspections. Her work involves collaborating with Paul Palmer to offer services such as QP declarations for API manufacturers, regulatory inspection hosting, commercial and clinical batch release, compliance audits, and coaching and training in GxP.
NEW higher discounts for multiple bookings - bring your colleagues to make your training budget go further:
- 30% off the 2nd delegate*
- 40% off the 3rd delegate*
- 50% off the 4th delegate*
Please contact us for pricing if you are interested in booking 5 or more delegates
24-25 July 2024
Live online
09:30-17:30 UK (London) (UTC+01)
10:30-18:30 Paris (UTC+02)
04:30-12:30 New York (UTC-04)
Course code 13835
- GBP 1,099 1,299
- EUR 1,579 1,859
- USD 1,786 2,098
Until 19 Jun
- 2 days live online training
- Browser-based, no download usually required
- See presenters and interact with fellow attendees
- Download documentation and certification of completion
- Fair transfer and cancellation policy
Not ready to book yet?
for 7 days, no obligation
25-26 November 2024
Live online
09:30-17:30 UK (London) (UTC+00)
10:30-18:30 Paris (UTC+01)
04:30-12:30 New York (UTC-05)
Course code 14053
- GBP 1,099 1,299
- EUR 1,579 1,859
- USD 1,786 2,098
Until 21 Oct
- 2 days live online training
- Browser-based, no download usually required
- See presenters and interact with fellow attendees
- Download documentation and certification of completion
- Fair transfer and cancellation policy
Not ready to book yet?
for 7 days, no obligation
* Early booking discounts may not be combined with other discounts or offers. As such, the discounts for 2nd/3rd/4th delegates are based on the full price; and apply only when booking multiple delegates on the same date.
Reviews of IPI's Understanding Computer System Validation (CSV) training course
My overall opinion is that this course was very worthwhile and well taught. I feel as though I learned a lot but I have learned in a way in which I will be able to apply this knowledge confidently to my job.
Jul 26 2023
Rachel Power 
R&D Project Technician, Teva Pharmaceuticals Europe BV
Jul 26 2023
Paul gave a very informative and interactive course. He made the learning enjoyable, and it was obvious how knowledgeable he was.
Brid Hogan
R&D Project associate, Teva Pharmaceuticals Europe BV
Jul 26 2023
Good, well presented and full of information and knowledge
Iti Sharma 
QA Assosiate, Nox Medical
United Kingdom
- Catalent Micron Technologies Limited
- PharSafer
Iceland
- Nox Medical
Ireland
- Teva Pharmaceuticals Europe BV
Netherlands
- Venn Life Sciences ED B.V.
Norway
- Gentian AS
