Topics
- Higher assurance of new medical product approvals
- Achieve satisfactory inspections more easily
- Reduce rates of batch rework and rejections
- Minimize nonconformances
- Take a holistic approach to validation
- Avoid product recalls
- Achieve synergy among validation programs
Who should Attend
Regulatory affairs, QA managers and personnel, Engineers, Operations managers, Training departments, Validation professionals, Quality Engineers and Consultants.
