Ten-Step Process for COTS Computer System Validation - Reduce Time and Costs - GlobalCompliancePanel 2013
03 Apr 2013
Webinar
Key Topics
How to use the risk-based validation approach to lower costs
Learn which documents the FDA expects to audit
Document a computer system validation project using easy to understand fill-in-the-blank templates
How to link requirements, specifications, risk management, and testing
Step-by-step instructions for performing and documenting a risk assessment, and how to use the results to reduce validation documentation
Based on: "Risk-Based Software Validation - Ten Easy Steps" (Davis Horwood International and PDA - www.pda.org, 2006)
Reduce testing by writing test cases that trace to elements of risk management
Who should Attend
QA
IT
Laboratory Staff
QC
GMP, GCP, GLP professionals
Managers
Past Events
Ten-Step Process for COTS Computer System Validation - Reduce Time and Costs - GlobalCompliancePanel 2013 - 03 Apr 2013, Webinar (37621)
Ten-Step Process for COTS Computer System Validation - Reduce Time and Costs - GlobalCompliancePanel 2026
Important
Please, check "Ten-Step Process for COTS Computer System Validation - Reduce Time and Costs - GlobalCompliancePanel" official website for possible changes, before making any traveling arrangements
Event Categories
Health & Medicine: Healthcare, Medical technology, Pharma
