-Understand the elements of the and how each subsystem is interconnected to the rest in order to meet GMP requirements. -Conduct internal audits to monitor quality and apply corrective actions when appropriate. -Evaluate SOPs, design controls, and validation protocols from a quality perspective and make revisions or improvements as needed. -Organize and manage evaluation data to improve product quality and address customer complaints. Prices:General Admission: USD 1395.0General Admission: USD 2195.0 Time: 9:00 am - 5:00 pm Venue details: San Diego Training and Conference Center, 450 B St., San Diego, 92101, United States