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6-Hour Virtual Seminar on Validation and 21 CFR Part 11 Compliance of Computer Systems

March 18 @ 8:00 am - 2:00 pm CDT


This course is appropriate for beginner and experienced person alike. The topics will build on each other and will give you the latest trends in our heavily regulated industry and how to make it easy for yourself while still achieving data integrity.

The attendees will be given take away templates that will enable them to build a complete package to meet Data Integrity Requirements for Computerized Systems.

We have all heard of Computer Systems Validation & Data Integrity, but do you really understand what it is? Do you understand how 21 CFR 11 and Annex 11 fit into this picture? Specifically, can you answer questions on the following:

21 CFR Part 11 and Computer Validation: Why so many citations?
Computer Systems Validation (CSV) and 21 CFR 11 vs Annex 11
Data Integrity vs Computer Systems Validation
Overview and Key Requirements of Part 11 & CSV
How to use a Risk Based Assessment to reduce work while still achieving Compliance?
How FDA & other Regulatory Authorities Inspect Computerized Systems for Data Integrity?
Why you should attend
This course will provide the attendees with more detailed experience on validation / 21 CFR 11 compliance of a computer system, as well as details for activities associated with computer systems validation.

Who Will Benefit
VP of IT
Director of IT
Quality Managers
Project Managers (for DATA INTEGRITY / IT)
Validation Specialists
Database Administrators
System Administrators
Directors / Senior Directors of Discovery
Directors / Senior Directors of Development
Directors / Senior Directors of Commercialization
Document Managers
Training Managers
Data Managers
Safety Managers


Global Compliance Panel


online event
CA 94539 + Google Map