Discover process improvement and quality management within life sciences and pharmaceuticals.
-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.
ORGANIZATION BENEFITS:
Operate a GMP compliant manufacturing operation that supports changes to facilities,
equipment, and processes to support product improvement
Save money and ensure product quality by encouraging “quality by design”
Improve product safety and integrity through increased quality monitoring at all stages of the manufacturing process
Prepare for the FDA’s systems based inspection
Prices:
General Admission: USD 1395.0
General Admission: USD 2195.0
Time: 9:00 am - 5:00 pm
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