6-Hour Virtual Seminar on Qualification (IQ, OQ, PQ) and Validation of Laboratory Equipment and Systems for Regulated Industries (Pharma, Biotech, Devices, etc.)
6-Hour Virtual Seminar on Risk Based Scientific Approach to Analytical Method Development and Validation Activities for Regulated Laboratories
6-Hour Virtual Seminar on GxP/GMP and its Consequences for Quality Management, Quality Audit, Documentation, and Information Technology Systems
6-Hour Virtual Seminar - Evolution of the Quality Management System - How to go from Surviving to Thriving
6-Hour Virtual Seminar on FDA Trends for Computer System Validation (CSV) Compliance and Enforcement
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