Two Day Computer System Validation Seminar: Reduce Costs and Avoid 483s: (Burlingame CA, United States - November 2nd-3rd, 2017)

This Computer System Validation Training course will explore proven techniques for reducing costs associated with implementing, using, and maintaining computer systems in regulated environments. Today, the FDA performs both GxP and Part 11 inspections, the Europeans have released an updated Annex 11 regulation that expands Part 11 requirements and companies must update their systems and processes to maintain compliance.

This Computer System Validation Training course will explore proven techniques for reducing costs associated with implementing, using, and maintaining computer systems in regulated environments. Today, the FDA performs both GxP and Part 11 inspections, the Europeans have released an updated Annex 11 regulation that expands Part 11 requirements and companies must update their systems and processes to maintain compliance.

Many companies outsource IT resources and are involved in Software as a Service (SaaS) and cloud computing. These vendors are not regulated, and therefore, regulated companies must ensure compliance for both infrastructure qualification and computer system validation to avoid FDA form 483s and Warning Letters.

This Computer System Validation Training course is intended for these regulated companies, software vendors, and SaaS/cloud providers.

The seminar instructor will:

Learning Objective:

For more information about this conference visit https://www.researchandmarkets.com/research/lwgqxt/computer_system

Media Contact:

Research and Markets
Laura Wood, Senior Manager
press@researchandmarkets.com

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