Overview
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Learn about computerized system validation (CSV) requirements for GMP and GLP laboratories in this 32-minute webinar presented by analytical chemist Dr. Bob McDowall. Explore risk-based validation approaches that ensure regulatory compliance while leveraging supplier software development and testing to reduce validation workload. Discover how to move beyond inflexible, one-size-fits-all validation methods toward more efficient strategies for Laboratory Information Management Systems (LIMS) and other laboratory systems. Understand the regulatory landscape that has required CSV for over 40 years and gain practical insights from an expert with over 50 years of analytical chemistry experience and 35+ years in computerized system validation. Earn PACE credits by completing the webinar and following the provided certification process through Labroots.
Syllabus
The Importance of Validating LIMS and Laboratory Systems
Taught by
Labroots