Computer System Validation Course
What will I learn?
Master the essentials of Computer System Validation with our comprehensive course tailored for Operations professionals. Delve into regulatory frameworks like FDA 21 CFR Part 11 and GAMP 5, and learn to develop robust validation plans. Gain hands-on experience in executing and documenting tests, assessing risks, and designing test protocols. Enhance your skills in preparing validation reports, ensuring compliance, and addressing deviations. Elevate your expertise and ensure your systems meet industry standards efficiently.
Apoia's Differentials
Develop skills
Strengthen the development of the practical skills listed below
Master regulatory frameworks: Navigate FDA 21 CFR Part 11 and GAMP 5.
Develop validation plans: Define scope, objectives, and timelines effectively.
Execute test protocols: Conduct and document functional, security, and performance tests.
Assess risks: Identify, document, and mitigate potential system validation risks.
Prepare validation reports: Ensure compliance and present clear, concise results.
Suggested summary
Workload: between 4 and 360 hours
Before starting, you can adjust the chapters and the workload.
- Choose which chapter to start with
- Add or remove chapters
- Increase or decrease the course workload
Examples of chapters you can add
You will be able to generate more chapters like the examples below
This is a free course, focused on personal and professional development. It is not equivalent to a technical, undergraduate, or postgraduate course, but offers practical and relevant knowledge for your professional journey.