-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.
General Admission: USD 1395.0
General Admission: USD 2195.0
Time: 9:00 am - 5:00 pm
Venue details: San Diego Training and Conference Center