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Computerised Systems Validation Course
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Computerised Systems Validation Course

Master the full lifecycle of Computerised Systems Validation — from regulatory foundations and risk assessment to cloud-based systems and inspection readiness. This course equips quality, IT, and compliance professionals with the practical skills to build, execute, and maintain compliant validation programmes. Stay audit-ready and protect product quality at every stage.

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What your team will master:

This course covers every phase of computerised systems validation, starting with regulatory requirements and the V-model lifecycle, then moving through risk-based scoping, documentation, and qualification protocols. You will learn to write User Requirements Specifications, build traceability matrices, and execute IQ, OQ, PQ, and UAT protocols. Data integrity principles under ALCOA+ are addressed in depth, along with audit trail configuration and electronic records management. You will also gain practical skills in change control, revalidation, cloud and SaaS validation, and inspection readiness. Advanced topics include Agile and DevOps integration, validation metrics, and emerging technologies such as AI and IoT in regulated environments.

How your team learns practically Computerised Systems Validation Course

How your team practises Computerised Systems Validation Course

Professionals from these companies study at Dedika

ActemiumFR
Nunner LogisticsNL
GT Constructora GeotécnicaCR
Sydel StarBR
Metrô de São PauloBR
Aguas AndinasCL
DSMIN
MeridianbetRS
CDHCN

Course content

8 Chapters • 36 LessonsDuration between 4 and 360 hours (you decide)

Chapter 1See details

Foundations of Computerised Systems Validation

  • Lesson 1 • The Validation Lifecycle Model

    Introduces the V-model and lifecycle phases from concept to retirement. Frames all subsequent chapters within a structured development and validation process.

  • Lesson 2 • Regulatory Drivers for Validation

    Covers the global regulatory expectations that mandate computerised system validation. Connects compliance obligations to real-world quality and patient safety outcomes.

  • Lesson 3 • Categories of Computerised Systems

    Classifies systems by function, complexity, and regulatory impact. Enables learners to identify which validation approach applies to a given system.

  • Lesson 4 • Core Validation Concepts and Terminology

    Defines essential vocabulary including validation, verification, qualification, and traceability. Provides a shared language used throughout the entire course.

Chapter 2See details

Risk-Based Approach to Validation

  • Lesson 1 • Defining Validation Scope Through Risk

    Translates risk assessment results into validation scope decisions and test coverage. Prevents over- or under-validation by anchoring scope to documented risk.

  • Lesson 2 • Risk Assessment Techniques

    Covers FMEA, risk ranking, and impact assessment tools applied to system functions. Learners select and apply the appropriate technique for a given system type.

  • Lesson 3 • Risk Management Principles in Validation

    Introduces formal risk management frameworks adapted for computerised systems. Establishes risk thinking as the foundation for all validation planning decisions.

  • Lesson 4 • Maintaining a Living Risk Register

    Establishes practices for updating risk assessments throughout the system lifecycle. Ensures validation remains current as systems and regulations evolve.

Chapter 3See details

Validation Planning and Documentation

  • Lesson 1 • Requirements Documentation

    Teaches writing unambiguous User Requirements Specifications and Functional Specifications. Good requirements are the basis for traceable, defensible test protocols.

  • Lesson 2 • Traceability Matrix Construction

    Builds forward and backward traceability from requirements through testing to results. Demonstrates complete coverage and supports regulatory inspection readiness.

  • Lesson 3 • Document Control in Validation

    Applies document management principles to validation deliverables including version control and audit trails. Ensures all validation records are retrievable and trustworthy.

  • Lesson 4 • System-Level Validation Plans

    Covers the content and approval requirements for a project-specific Validation Plan. Learners learn to tailor plans to system complexity and risk level.

  • Lesson 5 • The Validation Master Plan

    Defines the purpose, scope, and structure of a site-level Validation Master Plan. Connects site strategy to individual system validation projects.

Chapter 4See details

Installation and Operational Qualification

  • Lesson 1 • Installation Qualification Principles

    Defines IQ objectives and the evidence required to confirm correct system installation. Establishes the physical and environmental baseline for all subsequent testing.

  • Lesson 2 • Writing Effective IQ Protocols

    Guides learners through drafting step-by-step IQ test scripts with acceptance criteria. Emphasises clarity and objectivity so any qualified tester can execute consistently.

  • Lesson 3 • Operational Qualification Principles

    Defines OQ objectives and the functional tests that confirm system operation within specified limits. Bridges installation verification to performance-level testing.

  • Lesson 4 • Executing and Recording Qualification Tests

    Covers real-time execution practices, deviation handling, and contemporaneous record-keeping. Produces compliant, inspection-ready qualification records.

  • Lesson 5 • IQ and OQ Summary Reports

    Teaches writing qualification summary reports that evaluate results against acceptance criteria. Provides the formal basis for proceeding to performance qualification.

Chapter 5See details

Performance Qualification and User Acceptance Testing

  • Lesson 1 • Performance Qualification Design

    Defines PQ objectives and the process-representative scenarios that prove consistent performance. Distinguishes PQ from OQ by focusing on end-to-end business processes.

  • Lesson 2 • User Acceptance Testing Strategy

    Positions UAT as the business owner's confirmation that the system meets user requirements. Aligns UAT with PQ to avoid duplication while ensuring full coverage.

  • Lesson 3 • Executing PQ and UAT Protocols

    Covers execution logistics, data integrity during testing, and managing unexpected results. Ensures test execution produces reliable, attributable, and complete records.

  • Lesson 4 • Evaluating and Closing Qualification

    Guides evaluation of PQ and UAT results and preparation of the final qualification report. Formal closure authorises system release for intended use.

Chapter 6See details

Data Integrity in Computerised Systems

  • Lesson 1 • Remediation of Data Integrity Gaps

    Provides a structured approach to investigating and correcting identified data integrity deficiencies. Produces a CAPA plan that satisfies regulatory remediation expectations.

  • Lesson 2 • ALCOA+ Framework and Principles

    Defines Attributable, Legible, Contemporaneous, Original, Accurate, and extended attributes. Provides the evaluative standard applied to all electronic records and audit trails.

  • Lesson 3 • Audit Trail Requirements and Review

    Covers the design, configuration, and periodic review of system audit trails. Ensures that all data creation, modification, and deletion events are captured and reviewable.

  • Lesson 4 • Data Integrity Risk Assessment

    Applies risk assessment methodology specifically to data flows and storage within a system. Identifies vulnerabilities and prioritises controls to prevent data manipulation.

  • Lesson 5 • Electronic Records and Signatures

    Addresses requirements for electronic records to be equivalent to paper records and signatures. Learners configure and verify electronic signature controls within validated systems.

Chapter 7See details

Change Control and Revalidation

  • Lesson 1 • Executing Revalidation Activities

    Covers planning and executing targeted revalidation protocols following approved changes. Ensures only affected functions are retested while maintaining full traceability.

  • Lesson 2 • Impact Assessment for System Changes

    Teaches structured evaluation of how a proposed change affects validated functions and data. Determines the extent of revalidation required before implementation.

  • Lesson 3 • Change Control Process Overview

    Defines the formal change control workflow from request through approval and implementation. Establishes change control as the mechanism protecting the validated state.

  • Lesson 4 • Periodic Review of Validated Systems

    Establishes a scheduled review process to confirm systems remain in a validated state over time. Identifies drift, uncontrolled changes, and emerging risks between formal changes.

Chapter 8See details

Validation of Cloud and SaaS Systems

  • Lesson 1 • Vendor Assessment and Qualification

    Covers auditing cloud vendors and leveraging their documentation to support user validation. Establishes the supplier qualification process as a prerequisite to system validation.

  • Lesson 2 • Continuous Validation in Agile SaaS Updates

    Adapts validation practices to frequent vendor-driven updates in SaaS environments. Produces a sustainable update assessment process that maintains the validated state.

  • Lesson 3 • Data Integrity and Security in the Cloud

    Addresses data residency, backup, recovery, and access control requirements for cloud-hosted data. Ensures ALCOA+ compliance is maintained when data is stored off-premises.

  • Lesson 4 • Cloud Deployment Models and Validation Impact

    Distinguishes IaaS, PaaS, and SaaS models and their effect on validation responsibilities. Maps which qualification activities shift to the vendor versus remain with the user organisation.

  • Lesson 5 • Configuration and Validation in SaaS

    Focuses validation effort on configurable elements within SaaS platforms rather than underlying code. Learners identify and test all configuration decisions that affect regulated processes.

Certification

Your valid completion certificate

This course is for you:

  • Quality assurance specialists: seeking structured expertise in regulated system validation.

  • IT professionals in pharma or biotech: bridging technical skills with compliance requirements.

  • Regulatory affairs coordinators: expanding their scope to include computerised system oversight.

  • Validation engineers early in their careers: building a defensible, audit-ready skill set.

  • Manufacturing operations managers: responsible for systems that touch product quality decisions.

  • Compliance consultants: formalising their CSV knowledge to serve regulated industry clients.

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