Skip to main content

Skillbee Solution

Announcement
A P J Abdul Kalam University Affiliated Institute & ISO 9001:2015 Certified Institute

Computer System Validation Course In UK

3-Month Online Training | CSV • CSA • GAMP 5 • 21 CFR Part 11

A Practical Guide to Computer System Validation in Pharma

Computer System Validation (CSV) is more than a compliance requirement. In pharmaceutical and other regulated environments, a structured validation approach helps organizations demonstrate that computerized systems are suitable for their intended use, support reliable data and remain controlled throughout their lifecycle.

CSV can also improve project implementation by creating a clear framework for requirements, risk assessment, testing, documentation, approvals and lifecycle controls. This makes validation relevant not only to Quality Assurance and Validation teams, but also to IT, Informatics, Quality Control, R&D, Procurement, Compliance and business users.

Why Choose a CSV Course in UK?

UK is an important technology and life-sciences hub. A Computer System Validation Course in UK is relevant for learners who want to understand how software, IT infrastructure and pharmaceutical quality systems come together in regulated environments. The online format allows participants to develop CSV knowledge while learning from anywhere in the city.

What Does a CSV Professional Need to Understand?

  • Intended use and user requirements
  • GxP impact and risk assessment
  • Software categorization
  • Validation planning and documentation
  • Functional and technical specifications
  • Test planning and execution
  • IQ, OQ, PQ and UAT
  • Defect and change management
  • Data integrity and audit trails
  • Cloud and infrastructure qualification
  • Periodic review and system retirement
  • Computer Software Assurance (CSA)

Course Structure: Core Modules

  1. Module 1: Software Validation & Infrastructure Qualification
  2. Module 2: Computer System Validation (CSV): Overview, GAMP 5, 21 CFR Part 11 and documentation
  3. Module 3: High Level Risk Assessment: GxP Assessment, Software Categorization and ERES Assessment
  4. Module 4: GAMP 5 Documentation: URS, FS, DS, CS, Source Code Review Report, Validation Plan, Validation Report, Test Plan and Test Summary Report
  5. Module 5: Testing of Computerized Systems: IQ, OQ, PQ, UAT, Regression, Smoke and Sanity Testing
  6. Module 6: Penetration Testing: Threat Modeling, SAST and DAST
  7. Module 7: Excel Sheet Validation
  8. Module 8: Cloud Computing: SaaS, PaaS and IaaS
  9. Module 9: Software Development Life Cycle: Waterfall, V-Model, Agile and DevOps
  10. Module 10: Backup and Restore, Archival and Retrieval of Data
  11. Module 11: Business Continuity Management
  12. Module 12: System Retirement and Data Migration
  13. Module 13: Quality Management System and Quality Risk Management
  14. Module 14: Computer Software Assurance (CSA): A New Way of Working for CSV
  15. Module 15: URS / FRS / PRS / SRS
  16. Module 16: Source Code Review Report: Live Understanding
  17. Module 17: Infrastructure Qualification: Physical and Cloud
  18. Module 18: Software Testing Lifecycle (STLC)
  19. Module 19: System or Software Categorization Checklist
  20. Module 20: Test Management Tools: Live Hands-on Experience
  21. Module 21: Defect Management Tools: Live Hands-on Experience
  22. Module 22: Test Summary Report and Validation Summary Report
  23. Module 23: Validation Deliverables: Category 3, 4 and 5, with Live Hands-on Experience
  24. Module 24: Operation / Maintenance of Software
  25. Module 25: Periodic Review of Software
  26. Module 26: Decommissioning of Software
  27. Module 27: Data Migration
  28. Module 28: GAMP 5 Guideline
  29. Module 29: PLC Validation

Advanced Topics

  • Module 30: Virtual Machine (VM)
  • Module 31: DevOps Structure
  • Module 32: Deployment / Delivery / Hosting: CI/CD Approach
  • Module 33: Disaster Recovery, Business Continuity and IT Resilience Plan
  • Module 34: GAMP 5 Comparison between 1st and 2nd Version
  • Module 35: Artificial Intelligence and its Validation Approach
  • Module 36: Excel Sheet Validation
  • Module 37: Data Integrity and Data Integrity Checklist
  • Module 38: Software Designing: Database, Backend and Front End
  • Module 39: Cloud Computing: IaaS, PaaS and SaaS
  • Module 40: Computer Software Assurance (CSA)
  • Module 41: Agile Project & Sprint Creation: Agile and SCRUM concepts
  • Module 42: GAMP 5 Comparison between 1st and 2nd Version
  • Module 43: Infrastructure as Code
  • Module 44: Different IT Terminologies

Live Project Exposure

The supplied programme content includes practical teaching around:

  • Data Acquisition System (DAS)
  • Chromatographic Data System (CDS)
  • Packing US-Serialization System

From URS to Validation Report: Understanding the Lifecycle

A validation project normally begins with understanding intended use and user requirements. Risk assessment then helps determine the appropriate validation approach. Specifications and configuration or development activities are followed by testing and qualification. Evidence is documented through approved protocols, executed test records, deviations or defects where applicable, traceability and final reports. After release, the validated state must be maintained through controlled operation, change management, periodic review and, eventually, retirement or migration.

GAMP 5, 21 CFR Part 11 and CSA

The course introduces GAMP 5 as a risk-based framework used in computerized system validation, 21 CFR Part 11 concepts for electronic records and electronic signatures, and Computer Software Assurance as a modern risk-based approach to establishing confidence in software used in regulated processes.

Testing and Quality Evidence

Participants are introduced to IQ, OQ, PQ and UAT along with regression, smoke and sanity testing. The programme also covers test management, defect management, Test Summary Reports and Validation Summary Reports. These topics help learners understand how objective evidence is generated and organized during a validation project.

Modern CSV: Cloud, DevOps, AI and Data Integrity

Modern computerized systems increasingly use cloud platforms, virtual machines, DevOps pipelines, automated deployment, connected databases and artificial intelligence. Validation teams therefore need awareness of infrastructure, vendor responsibilities, cybersecurity, data integrity, deployment controls and lifecycle risks. The advanced modules introduce these areas, including IaaS, PaaS, SaaS, CI/CD, infrastructure as code and AI validation.

Who Can Benefit from This Training?

The supplied course content identifies professionals in Quality Assurance, Compliance, Validation, Informatics, Procurement, R&D, Commercial and Quality Control as potential beneficiaries. It is also relevant to people working with vendors, regulated computerized systems, audits and regulatory agencies.

Course Snapshot

Course

Computer System Validation Course

Location Focus

UK

Duration

3 Months

Training Mode

Online

Certification

Yes

Placement Assistance

Provided

Assessment & Certification

Participants are expected to appear for the applicable online assessment. After successfully qualifying according to the programme requirements, participants will be certified by Skillbee Solution.

Placement Assistance & Career Support

Skillbee Solution states that it provides job placement support, resume building, interview sessions and online support. Its website also describes live-project learning as part of its training approach.

How to Apply

All the participants are expected to appear for online assessment. After successfully qualifying the examination Computer System Validation Course Online, the participants will be certified by SkillBee Solution. Enrol in our e-Learn Computer System Validation training course in Pharma Industry, suitable for both beginners and professionals, with training available in Bangalore, Hyderabad, USA and UK

Start your Computerized System Validation journey Today!

Frequently Asked Questions

What is Computer System Validation?

CSV is a structured, documented process used to provide evidence that computerized systems are suitable for their intended use and perform as expected in regulated environments.

What is the duration?

The course duration is 3 months.

Is the training online?

Yes, the programme is delivered online.

Does the course cover GAMP 5?

Yes, GAMP 5 is covered in the core modules and advanced topics.

Does it cover 21 CFR Part 11?

Yes, the programme introduces 21 CFR Part 11 and electronic records/electronic signatures.

Is CSA included?

Yes. Computer Software Assurance is covered as a dedicated module and advanced topic.

Is Excel Sheet Validation included?

Yes. Excel Sheet Validation is included in the programme.

Are live projects included?

Are live projects included?
The supplied programme content identifies DAS, CDS and Packing US-Serialization System as live project teaching areas.

Is certification provided?

Yes, following the applicable assessment and completion requirements.

Is placement assistance available?

Yes, placement assistance is provided.